A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520796



Internal ID15448089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89247713..89250722hg38UCSC Ensembl
Innerchr10:91007470..91010479hg19UCSC Ensembl
Innerchr10:90997450..91000459hg18UCSC Ensembl
Innerchr10:90997450..91000459hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg383010
hg193010
hg183010
hg173010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689951, nssv681476, nssv693238, nssv675559
Samples
Known GenesLIPA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520796
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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