A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525712



Internal ID15453005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91046715..91071682hg38UCSC Ensembl
Innerchr10:92806472..92831439hg19UCSC Ensembl
Innerchr10:92796452..92821419hg18UCSC Ensembl
Innerchr10:92796452..92821419hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3824968
hg1924968
hg1824968
hg1724968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701874
Samples
Known GenesLINC00502
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525712
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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