A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2567992



Internal ID17845261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132250538..132258399hg38UCSC Ensembl
Innerchr9:135125925..135133786hg19UCSC Ensembl
Innerchr9:134115746..134123607hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg387862
hg197862
hg187862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982351
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2567992
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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