A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945716



Internal ID18592567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:359393..380649hg38UCSC Ensembl
Innerchr1:438688..459944hg19UCSC Ensembl
Innerchr1:428551..449807hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3821257
hg1921257
hg1821257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1755742, nssv1755733, nssv1755738, nssv1755741, nssv1755734, nssv1755737, nssv1755740, nssv1755736, nssv1755735, nssv1755739
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945716
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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