A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3464069



Internal ID19060491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:81269369..81297735hg38UCSC Ensembl
Innerchr1:81735054..81763420hg19UCSC Ensembl
Innerchr1:81507642..81536008hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3828367
hg1928367
hg1828367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000126
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)nssv3464069
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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