A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739553



Internal ID18691148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3969405..4188819hg38UCSC Ensembl
Innerchr3:4011089..4230503hg19UCSC Ensembl
Innerchr3:3986089..4205503hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38219415
hg19219415
hg18219415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001115
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)nssv3739553
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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