A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523409



Internal ID15104016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37335713..37339971hg38UCSC Ensembl
Innerchr7:37375317..37379575hg19UCSC Ensembl
Innerchr7:37341842..37346100hg18UCSC Ensembl
Innerchr7:37148557..37152815hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384259
hg194259
hg184259
hg174259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv420n21
Supporting Variantsnssv699160
Samples
Known GenesELMO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523409
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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