A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3481726



Internal ID19069851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27020286..27098402hg38UCSC Ensembl
Innerchr1:27346777..27424893hg19UCSC Ensembl
Innerchr1:27219364..27297480hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3878117
hg1978117
hg1878117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005755
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)nssv3481726
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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