A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609419



Internal ID16050142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158712157..159117938hg38UCSC Ensembl
Innerchr7:158504848..158910629hg19UCSC Ensembl
Innerchr7:158197609..158603390hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38405782
hg19405782
hg18405782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1102021
Samples
Known GenesESYT2, LINC00689, VIPR2, WDR60
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609419
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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