A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2539113



Internal ID17752853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42601409..42618696hg38UCSC Ensembl
Innerchr9:44278214..44295494hg19UCSC Ensembl
Innerchr9:44218210..44235490hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3817288
hg1917281
hg1817281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972351
Supporting Variants
SamplesHGDP00521
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)nssv2539113
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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