A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582006



Internal ID18880287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76317328..76355201hg38UCSC Ensembl
Innerchr2:76544454..76582327hg19UCSC Ensembl
Innerchr2:76397962..76435835hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3837874
hg1937874
hg1837874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007312
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)nssv3582006
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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