A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945719



Internal ID18245884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:585989..588370hg38UCSC Ensembl
Innerchr1:521369..523750hg19UCSC Ensembl
Innerchr1:510953..513613hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg382382
hg192382
hg182661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2n82
Supporting Variantsnssv1749512, nssv1749510, nssv1749513, nssv1749509, nssv1749507, nssv1749514, nssv1749508, nssv1749515, nssv1749511, nssv1749506
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)nsv945719
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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