A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972031



Internal ID18607247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:57867118..57870418hg38UCSC Ensembl
Innerchr11:57634590..57637890hg19UCSC Ensembl
Innerchr11:57391166..57394466hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg383301
hg193301
hg183301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1889807, nssv1889805, nssv1889802, nssv1889809, nssv1889808, nssv1889804, nssv1889803, nssv1889811, nssv1889810, nssv1889806
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)nsv972031
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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