A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521269



Internal ID15101876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46001360..46080288hg38UCSC Ensembl
Innerchr10:51515534..51594462hg19UCSC Ensembl
Innerchr10:51185540..51264468hg18UCSC Ensembl
Innerchr10:51185540..51264468hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3878929
hg1978929
hg1878929
hg1778929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697878
Samples
Known GenesMSMB, NCOA4, TIMM23
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521269
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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