A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527837



Internal ID8422112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113128849..113151320hg38UCSC Ensembl
Innerchr10:114888608..114911079hg19UCSC Ensembl
Innerchr10:114878598..114901069hg18UCSC Ensembl
Innerchr10:114878598..114901069hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3822472
hg1922472
hg1822472
hg1722472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704335
Samples
Known GenesTCF7L2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527837
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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