A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669898



Internal ID15406550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46325178hg38UCSC Ensembl
Innerchr10:47543322..47696414hg19UCSC Ensembl
Innerchr10:47013328..47166420hg18UCSC Ensembl
Innerchr10:47013328..47166420hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38153093
hg19153093
hg18153093
hg17153093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669898
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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