A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2527831



Internal ID17816767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35505261..35509524hg38UCSC Ensembl
Innerchr9:35505258..35509521hg19UCSC Ensembl
Innerchr9:35495258..35499521hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384264
hg194264
hg184264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968610
Supporting Variants
SamplesHGDP00927
Known GenesRUSC2
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)nssv2527831
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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