A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945839



Internal ID18592689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26126760..26129641hg38UCSC Ensembl
Innerchr1:26453251..26456132hg19UCSC Ensembl
Innerchr1:26325838..26328719hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382882
hg192882
hg182882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765343, nssv1765346, nssv1764415, nssv1765340, nssv1765345, nssv1765344, nssv1765342, nssv1765341, nssv1765347, nssv1765348
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)nsv945839
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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