A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2539403



Internal ID17820003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42663831..42672519hg38UCSC Ensembl
Innerchr9:44340634..44349318hg19UCSC Ensembl
Innerchr9:44280630..44289314hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388689
hg198685
hg188685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv968649
Supporting Variants
SamplesHGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2539403
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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