A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436987



Internal ID15383228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110088850..110089691hg38UCSC Ensembl
Outerchr5:110085330..110090799hg38UCSC Ensembl
Innerchr5:109424551..109425392hg19UCSC Ensembl
Outerchr5:109421031..109426500hg19UCSC Ensembl
Innerchr5:109452450..109453291hg18UCSC Ensembl
Outerchr5:109448930..109454399hg18UCSC Ensembl
Innerchr5:109500767..109501608hg16UCSC Ensembl
Outerchr5:109497247..109502716hg16UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg385470
hg195470
hg185470
hg165470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466868
SamplesNA10839
Known Genes
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv436987
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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