A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920102



Internal ID16214058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:137030106..137132895hg38UCSC Ensembl
Innerchr2:137787676..137890465hg19UCSC Ensembl
Innerchr2:137504146..137606935hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38102790
hg19102790
hg18102790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583178
Supporting Variants
Samples
Known GenesTHSD7B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv920102
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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