A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2069822



Internal ID17407154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87933732..87936792hg38UCSC Ensembl
Innerchr16:87967338..87970398hg19UCSC Ensembl
Innerchr16:86524839..86527899hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383061
hg193061
hg183061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv984362
Supporting Variants
SamplesHGDP00521
Known GenesCA5A
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)nssv2069822
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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