A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591613



Internal ID18543208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4132155..4271801hg38UCSC Ensembl
Innerchr3:4173839..4313485hg19UCSC Ensembl
Innerchr3:4148839..4288485hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38139647
hg19139647
hg18139647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006352
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)nssv3591613
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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