A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2532302



Internal ID17809200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39397594..39412910hg38UCSC Ensembl
Innerchr9:39397591..39412907hg19UCSC Ensembl
Innerchr9:39387591..39402907hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3815317
hg1915317
hg1815317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982223
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)nssv2532302
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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