A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704612



Internal ID15094578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160839824..160844052hg38UCSC Ensembl
Innerchr5:160266831..160271059hg19UCSC Ensembl
Innerchr5:160199409..160203637hg18UCSC Ensembl
Innerchr5:160199409..160203637hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384229
hg194229
hg184229
hg174229
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528076
Supporting Variants
Samples
Known GenesATP10B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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