A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2535105



Internal ID17883727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39831978..39841768hg38UCSC Ensembl
Innerchr9:41976996..41986786hg19UCSC Ensembl
Innerchr9:41966996..41976786hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg389791
hg199791
hg189791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv968635
Supporting Variants
SamplesHGDP01307
Known GenesKGFLP2
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)nssv2535105
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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