A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521885



Internal ID15102492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1070731..1071574hg38UCSC Ensembl
Innerchr10:1116671..1117514hg19UCSC Ensembl
Innerchr10:1106671..1107514hg18UCSC Ensembl
Innerchr10:1106671..1107514hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38844
hg19844
hg18844
hg17844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694107
Samples
Known GenesWDR37
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521885
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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