A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466682



Internal ID19061894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40883580..40925041hg38UCSC Ensembl
Innerchr1:41349252..41390713hg19UCSC Ensembl
Innerchr1:41121839..41163300hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3841462
hg1941462
hg1841462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006158
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)nssv3466682
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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