A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975159



Internal ID18610367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19411406..19419500hg38UCSC Ensembl
Innerchr11:19432953..19441047hg19UCSC Ensembl
Innerchr11:19389529..19397623hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg388095
hg198095
hg188095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1879266, nssv1879273, nssv1879274, nssv1879270, nssv1879275, nssv1879267, nssv1879269, nssv1879272, nssv1879268, nssv1879271
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNAV2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975159
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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