A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972436



Internal ID18607652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100974597..100976759hg38UCSC Ensembl
Innerchr9:103736879..103739041hg19UCSC Ensembl
Innerchr9:102776700..102778862hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382163
hg192163
hg182163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563400, nssv2563399, nssv2563404, nssv2563403, nssv2563402, nssv2563397, nssv2563401, nssv2563396, nssv2563405, nssv2563398
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)nsv972436
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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