A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606674



Internal ID16394083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38579748..38616158hg38UCSC Ensembl
Innerchr7:38619348..38655758hg19UCSC Ensembl
Innerchr7:38585873..38622283hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3836411
hg1936411
hg1836411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1082841
Samples
Known GenesAMPH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606674
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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