A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972444



Internal ID18607660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114694913..114696720hg38UCSC Ensembl
Innerchr9:117457193..117459000hg19UCSC Ensembl
Innerchr9:116497014..116498821hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381808
hg191808
hg181808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2565955, nssv2565952, nssv2565947, nssv2565949, nssv2565950, nssv2565953, nssv2565951, nssv2565956, nssv2565954, nssv2565948
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)nsv972444
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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