A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982356



Internal ID18617551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19662..22515hg38UCSC Ensembl
Innerchr9:19662..22515hg19UCSC Ensembl
Innerchr9:9662..12515hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg382854
hg192854
hg182854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2724425, nssv2724418, nssv2724421, nssv2724422, nssv2724419, nssv2724427, nssv2724423, nssv2724420, nssv2724424, nssv2724426
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWASH1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982356
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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