A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696781



Internal ID15433433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130588286..130605918hg38UCSC Ensembl
Innerchr10:132386550..132404182hg19UCSC Ensembl
Innerchr10:132276540..132294172hg18UCSC Ensembl
Innerchr10:132276540..132294172hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3817633
hg1917633
hg1817633
hg1717633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516699
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696781
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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