A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2026358



Internal ID17501966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58150028..58155866hg38UCSC Ensembl
Innerchr15:58442227..58448065hg19UCSC Ensembl
Innerchr15:56229519..56235357hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385839
hg195839
hg185839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974582
Supporting Variants
SamplesHGDP01029
Known GenesAQP9
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)nssv2026358
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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