A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972428



Internal ID18607644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96721810..96727423hg38UCSC Ensembl
Innerchr9:99484092..99489705hg19UCSC Ensembl
Innerchr9:98523913..98529526hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg385614
hg195614
hg185614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561789, nssv2561784, nssv2561790, nssv2561785, nssv2561786, nssv2561788, nssv2561791, nssv2561792, nssv2561783, nssv2561787
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC441455
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972428
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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