A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2526726



Internal ID17871495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35956976..35958137hg38UCSC Ensembl
Innerchr9:35956973..35958134hg19UCSC Ensembl
Innerchr9:35946973..35948134hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381162
hg191162
hg181162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968611
Supporting Variants
SamplesHGDP01284
Known GenesOR2S2
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)nssv2526726
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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