A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517681



Internal ID15098288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94583471..94627322hg38UCSC Ensembl
Innerchr10:96343228..96387079hg19UCSC Ensembl
Innerchr10:96333218..96377069hg18UCSC Ensembl
Innerchr10:96333218..96377069hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3843852
hg1943852
hg1843852
hg1743852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652833, nssv676679
Samples
Known GenesHELLS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517681
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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