A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982342



Internal ID18617537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118082161..118083879hg38UCSC Ensembl
Innerchr9:120844439..120846157hg19UCSC Ensembl
Innerchr9:119884260..119885978hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg381719
hg191719
hg181719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563005, nssv2563002, nssv2563000, nssv2563008, nssv2563004, nssv2563006, nssv2562999, nssv2563007, nssv2563001, nssv2563003
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)nsv982342
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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