A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2533341



Internal ID17739043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41881598..41948354hg38UCSC Ensembl
Innerchr9:40283030..40349935hg19UCSC Ensembl
Innerchr9:40272921..40339935hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3866757
hg1966906
hg1867015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982229
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2533341
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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