A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606626



Internal ID16047349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38248669..38291209hg38UCSC Ensembl
Innerchr7:38288270..38330810hg19UCSC Ensembl
Innerchr7:38254795..38297335hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3842541
hg1942541
hg1842541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11275n54
Supporting Variantsnssv1082706, nssv1082705
Samples
Known GenesTARP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606626
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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