A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998628



Internal ID19158164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76703898..76727974hg38UCSC Ensembl
Innerchr1:77169583..77193659hg19UCSC Ensembl
Innerchr1:76942171..76966247hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3824077
hg1924077
hg1824077
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv199n100
Supporting Variantsnssv3482181, nssv3469345, nssv3468517, nssv3479353, nssv3468343, nssv3473122
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)nsv998628
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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