A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701874



Internal ID15438526
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 StatusS
Merged Variantsnsv525712
Supporting Variants
Samples
Known GenesLINC00502
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701874
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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