A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3463729



Internal ID19060316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40881523..40922990hg38UCSC Ensembl
Innerchr1:41347195..41388662hg19UCSC Ensembl
Innerchr1:41119782..41161249hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3841468
hg1941468
hg1841468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997467
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)nssv3463729
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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