A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437509



Internal ID15382815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:43077219..43110718hg38UCSC Ensembl
Outerchr6:43070325..43116036hg38UCSC Ensembl
Innerchr6:43044957..43078456hg19UCSC Ensembl
Outerchr6:43038063..43083774hg19UCSC Ensembl
Innerchr6:43152935..43186434hg18UCSC Ensembl
Outerchr6:43146041..43191752hg18UCSC Ensembl
Innerchr6:43091812..43125311hg16UCSC Ensembl
Outerchr6:43084918..43130629hg16UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3845712
hg1945712
hg1845712
hg1645712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467390
SamplesNA18521
Known GenesKLC4, PTK7
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)nsv437509
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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