A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747628



Internal ID15694898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46225568..46279254hg38UCSC Ensembl
Innerchr10:47596804..47650490hg19UCSC Ensembl
Innerchr10:47066810..47120496hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3853687
hg1953687
hg1853687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550783
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)nssv747628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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