A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527941



Internal ID15455234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57331978..57353643hg38UCSC Ensembl
Innerchr10:59091738..59113403hg19UCSC Ensembl
Innerchr10:58761744..58783409hg18UCSC Ensembl
Innerchr10:58761744..58783409hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3821666
hg1921666
hg1821666
hg1721666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704449
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527941
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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