A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2559813



Internal ID17786249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94281229..94288510hg38UCSC Ensembl
Innerchr9:97043511..97050792hg19UCSC Ensembl
Innerchr9:96083332..96090613hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387282
hg197282
hg187282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968732
Supporting Variants
SamplesHGDP00665
Known GenesZNF169
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)nssv2559813
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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