A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2557564



Internal ID17870365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87817074..87818550hg38UCSC Ensembl
Innerchr9:90431989..90433465hg19UCSC Ensembl
Innerchr9:89621809..89623285hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381477
hg191477
hg181477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982316
Supporting Variants
SamplesHGDP01284
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)nssv2557564
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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