A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151302



Internal ID15530798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:132451024..132495813hg38UCSC Ensembl
Innerchr2:133208597..133253386hg19UCSC Ensembl
Innerchr2:132925067..132969856hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3844790
hg1944790
hg1844790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583154
Supporting Variants
SamplesHGDP00998
Known GenesGPR39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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