A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2549929



Internal ID17507107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63776356..63918447hg38UCSC Ensembl
Innerchr9:68372090..68514181hg19UCSC Ensembl
Innerchr9:67861910..68004058hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38142092
hg19142092
hg18142149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968690
Supporting Variants
SamplesHGDP01029
Known GenesLOC642236
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)nssv2549929
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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