A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2535716



Internal ID17842065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39841768..39860766hg38UCSC Ensembl
Innerchr9:41986786..42005784hg19UCSC Ensembl
Innerchr9:41976786..41995784hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3818999
hg1918999
hg1818999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968636
Supporting Variants
SamplesHGDP00998
Known GenesKGFLP2, LOC643648
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)nssv2535716
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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