A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466714



Internal ID19061913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13988058..14044250hg38UCSC Ensembl
Innerchr1:14314553..14370745hg19UCSC Ensembl
Innerchr1:14187140..14243332hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3856193
hg1956193
hg1856193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006184
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)nssv3466714
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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