A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945874



Internal ID18592724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:33009986..33010919hg38UCSC Ensembl
Innerchr1:33475587..33476520hg19UCSC Ensembl
Innerchr1:33248174..33249107hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38934
hg19934
hg18934
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1759203, nssv1759210, nssv1759208, nssv1759202, nssv1759201, nssv1759204, nssv1759205, nssv1759207, nssv1759209, nssv1759206
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAK2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945874
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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