A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750038



Internal ID15697308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69384195..69415853hg38UCSC Ensembl
Innerchr10:71143951..71175609hg19UCSC Ensembl
Innerchr10:70813957..70845615hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3831659
hg1931659
hg1831659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551453
Supporting Variants
Samples
Known GenesHK1, TACR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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