A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972448



Internal ID18607664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122608100..122608753hg38UCSC Ensembl
Innerchr9:125370379..125371032hg19UCSC Ensembl
Innerchr9:124410200..124410853hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38654
hg19654
hg18654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2566348, nssv2566351, nssv2566349, nssv2566354, nssv2566352, nssv2566347, nssv2566353, nssv2566350, nssv2566346, nssv2566345
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)nsv972448
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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