A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2539059



Internal ID17841911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42740370..42803552hg38UCSC Ensembl
Innerchr9:44167567..44230749hg19UCSC Ensembl
Innerchr9:44107563..44170745hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3863183
hg1963183
hg1863183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972348
Supporting Variants
SamplesHGDP00998
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2539059
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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