A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697880



Internal ID15087846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50291885..50438087hg38UCSC Ensembl
Innerchr10:52051645..52197847hg19UCSC Ensembl
Innerchr10:51721651..51867853hg18UCSC Ensembl
Innerchr10:51721651..51867853hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38146203
hg19146203
hg18146203
hg17146203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521273
Supporting Variants
Samples
Known GenesSGMS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697880
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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