A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747376



Internal ID15694646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46166132..46281263hg38UCSC Ensembl
Innerchr10:47537368..47652499hg19UCSC Ensembl
Innerchr10:47007374..47122505hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38115132
hg19115132
hg18115132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550732
Supporting Variants
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747376
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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