A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174479



Internal ID15854042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46332377hg38UCSC Ensembl
Innerchr10:47543322..47703613hg19UCSC Ensembl
Innerchr10:47013328..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38160292
hg19160292
hg18160292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550755
Supporting Variants
Samples1780854537_A
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174479
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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