A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975200



Internal ID18610408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71566578..71569629hg38UCSC Ensembl
Innerchr11:71277624..71280675hg19UCSC Ensembl
Innerchr11:70955272..70958323hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383052
hg193052
hg183052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1894558, nssv1894567, nssv1894566, nssv1894565, nssv1894563, nssv1894562, nssv1894559, nssv1894560, nssv1894561, nssv1894564
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKRTAP5-10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975200
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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