A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971995



Internal ID18607211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23518721..23521213hg38UCSC Ensembl
Innerchr11:23540267..23542759hg19UCSC Ensembl
Innerchr11:23496843..23499335hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg382493
hg192493
hg182493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1879564, nssv1879566, nssv1879563, nssv1879560, nssv1879567, nssv1879558, nssv1879565, nssv1879562, nssv1879559, nssv1879561
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)nsv971995
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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