A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2556864



Internal ID17737685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90206184..90236424hg38UCSC Ensembl
Innerchr9:92968466..92998706hg19UCSC Ensembl
Innerchr9:92008286..92038526hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3830241
hg1930241
hg1830241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968726
Supporting Variants
SamplesHGDP00456
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)nssv2556864
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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