A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527065



Internal ID15454358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60496527..60499466hg38UCSC Ensembl
Innerchr10:62256285..62259224hg19UCSC Ensembl
Innerchr10:61926291..61929230hg18UCSC Ensembl
Innerchr10:61926291..61929230hg17UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg382940
hg192940
hg182940
hg172940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703444
Samples
Known GenesANK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527065
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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