A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2564720



Internal ID17838302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107167575..107170748hg38UCSC Ensembl
Innerchr9:109929856..109933029hg19UCSC Ensembl
Innerchr9:108969677..108972850hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383174
hg193174
hg183174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968744
Supporting Variants
SamplesHGDP00998
Known Genes
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)nssv2564720
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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