A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982195



Internal ID18617390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7477054..7478309hg38UCSC Ensembl
Innerchr9:7477054..7478309hg19UCSC Ensembl
Innerchr9:7467054..7468309hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381256
hg191256
hg181256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2521657, nssv2521658, nssv2521656, nssv2521661, nssv2521655, nssv2521654, nssv2521660, nssv2521653, nssv2521659, nssv2521662
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)nsv982195
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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