A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2534337



Internal ID17747973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60971677..60999027hg38UCSC Ensembl
Innerchr9:41557949..41585299hg19UCSC Ensembl
Innerchr9:41547949..41575299hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3827351
hg1927351
hg1827351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972699
Supporting Variants
SamplesHGDP00521
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)nssv2534337
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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