A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2562151



Internal ID17839955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109532666..109535007hg38UCSC Ensembl
Innerchr9:112294946..112297287hg19UCSC Ensembl
Innerchr9:111334767..111337108hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg382342
hg192342
hg182342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968747
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)nssv2562151
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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