A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972438



Internal ID18607654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101792300..101794010hg38UCSC Ensembl
Innerchr9:104554582..104556292hg19UCSC Ensembl
Innerchr9:103594403..103596113hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381711
hg191711
hg181711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2564537, nssv2564536, nssv2564538, nssv2564539, nssv2564540, nssv2564542, nssv2564545, nssv2564544, nssv2564541, nssv2564543
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)nsv972438
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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