A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971998



Internal ID18607214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32758092..32758592hg38UCSC Ensembl
Innerchr11:32779638..32780138hg19UCSC Ensembl
Innerchr11:32736214..32736714hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1881231, nssv1881227, nssv1881230, nssv1881232, nssv1881225, nssv1881223, nssv1881228, nssv1881226, nssv1881229, nssv1881224
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCDC73
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971998
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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