A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3467611



Internal ID19062404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13988058..14041670hg38UCSC Ensembl
Innerchr1:14314553..14368165hg19UCSC Ensembl
Innerchr1:14187140..14240752hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3853613
hg1953613
hg1853613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009457
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)nssv3467611
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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