A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973382



Internal ID18608597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97132449..97153789hg38UCSC Ensembl
Innerchr9:99894731..99916071hg19UCSC Ensembl
Innerchr9:98934552..98955892hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3821341
hg1921341
hg1821341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2752053, nssv2756305, nssv2747705, nssv2754249, nssv2750252, nssv2752931, nssv2754882, nssv2750402, nssv2753381, nssv2747492
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973382
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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