A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3727962



Internal ID19026243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22289612..22383088hg38UCSC Ensembl
Innerchr2:22512484..22605960hg19UCSC Ensembl
Innerchr2:22365989..22459465hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3893477
hg1993477
hg1893477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008106
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3727962
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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