A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173587



Internal ID15507739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46279254hg38UCSC Ensembl
Innerchr10:47543322..47650490hg19UCSC Ensembl
Innerchr10:47013328..47120496hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38107169
hg19107169
hg18107169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550742
Supporting Variants
Samples1780862109_A
Known GenesANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173587
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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