A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437413



Internal ID15382719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:17040390..17046242hg38UCSC Ensembl
Outerchr2:17037477..17060894hg38UCSC Ensembl
Innerchr2:17221657..17227509hg19UCSC Ensembl
Outerchr2:17218744..17242161hg19UCSC Ensembl
Innerchr2:17085138..17090990hg18UCSC Ensembl
Outerchr2:17082225..17105642hg18UCSC Ensembl
Innerchr2:17206170..17212022hg16UCSC Ensembl
Outerchr2:17203257..17226674hg16UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3823418
hg1923418
hg1823418
hg1623418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467294
SamplesNA12801
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)nsv437413
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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