A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2546600



Internal ID17809665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42988838..43075990hg38UCSC Ensembl
Innerchr9:66242575..66329727hg19UCSC Ensembl
Innerchr9:65982395..66069547hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3887153
hg1987153
hg1887153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972375
Supporting Variants
SamplesHGDP00778
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)nssv2546600
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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