A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174535



Internal ID15531724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46239982..46295928hg38UCSC Ensembl
Innerchr10:47611218..47667164hg19UCSC Ensembl
Innerchr10:47081224..47137170hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3855947
hg1955947
hg1855947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550792
Supporting Variants
SamplesHGDP01195
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174535
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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