A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2535812



Internal ID17809181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39877863..40101911hg38UCSC Ensembl
Innerchr9:42022881..42246929hg19UCSC Ensembl
Innerchr9:42012881..42236925hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38224049
hg19224049
hg18224045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982241
Supporting Variants
SamplesHGDP00778
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)nssv2535812
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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