A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174512



Internal ID15534011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46224041..46325790hg38UCSC Ensembl
Innerchr10:47595277..47697026hg19UCSC Ensembl
Innerchr10:47065283..47167032hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38101750
hg19101750
hg18101750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550780
Supporting Variants
SamplesNINDS_249
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174512
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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