A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591618



Internal ID18543213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4132155..4278113hg38UCSC Ensembl
Innerchr3:4173839..4319797hg19UCSC Ensembl
Innerchr3:4148839..4294797hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38145959
hg19145959
hg18145959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007955
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)nssv3591618
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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