A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946034



Internal ID18592884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:83363471..83489669hg38UCSC Ensembl
Innerchr1:83829154..83955352hg19UCSC Ensembl
Innerchr1:83601742..83727940hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38126199
hg19126199
hg18126199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1773618, nssv1773615, nssv1773624, nssv1773623, nssv1773621, nssv1773619, nssv1773616, nssv1773622, nssv1773620, nssv1773617
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)nsv946034
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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