A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591814



Internal ID18890095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6195885..6255943hg38UCSC Ensembl
Innerchr3:6237572..6297630hg19UCSC Ensembl
Innerchr3:6212572..6272630hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3860059
hg1960059
hg1860059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007794
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)nssv3591814
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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