A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739701



Internal ID19037982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37935209..37945425hg38UCSC Ensembl
Innerchr3:37976700..37986916hg19UCSC Ensembl
Innerchr3:37951704..37961920hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3810217
hg1910217
hg1810217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013731
Supporting Variants
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3739701
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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