A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2549055



Internal ID17395915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63743582..63776356hg38UCSC Ensembl
Innerchr9:68339316..68372090hg19UCSC Ensembl
Innerchr9:67829136..67861910hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3832775
hg1932775
hg1832775
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982287
Supporting Variants
SamplesHGDP00456
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)nssv2549055
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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