A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2538883



Internal ID17874634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42831967..42974083hg38UCSC Ensembl
Innerchr9:43997036..44139152hg19UCSC Ensembl
Innerchr9:43937032..44079148hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38142117
hg19142117
hg18142117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968643
Supporting Variants
SamplesHGDP01284
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2538883
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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