A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2543317



Internal ID17809983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62415164..62439954hg38UCSC Ensembl
Innerchr9:46726465..46751255hg19UCSC Ensembl
Innerchr9:46566461..46591251hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3824791
hg1924791
hg1824791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972366
Supporting Variants
SamplesHGDP00927
Known GenesKGFLP1
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)nssv2543317
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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