A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2037918



Internal ID17732920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96448104..96448820hg38UCSC Ensembl
Innerchr15:96991334..96992050hg19UCSC Ensembl
Innerchr15:94792338..94793054hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38717
hg19717
hg18717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977758
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)nssv2037918
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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