A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693457



Internal ID15083423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69801243..69818827hg38UCSC Ensembl
Innerchr10:71560999..71578583hg19UCSC Ensembl
Innerchr10:71231005..71248589hg18UCSC Ensembl
Innerchr10:71231005..71248589hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3817585
hg1917585
hg1817585
hg1717585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516370
Supporting Variants
Samples
Known GenesCOL13A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693457
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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