A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2539571



Internal ID17886827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42675671..42691195hg38UCSC Ensembl
Innerchr9:44352469..44368003hg19UCSC Ensembl
Innerchr9:44292465..44307999hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3815525
hg1915535
hg1815535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv968651
Supporting Variants
SamplesHGDP01307
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)nssv2539571
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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