A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv902732



Internal ID16196688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3376797..3390663hg38UCSC Ensembl
Innerchr2:3380568..3394434hg19UCSC Ensembl
Innerchr2:3359575..3373441hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3813867
hg1913867
hg1813867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580773
Supporting Variants
Samples
Known GenesTRAPPC12, TSSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv902732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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