A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2539295



Internal ID17776204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42621793..42631840hg38UCSC Ensembl
Innerchr9:44298592..44308643hg19UCSC Ensembl
Innerchr9:44238588..44248639hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810048
hg1910052
hg1810052
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv972717
Supporting Variants
SamplesHGDP00542
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)nssv2539295
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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