A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2037822



Internal ID17770365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96440779..96441902hg38UCSC Ensembl
Innerchr15:96984009..96985132hg19UCSC Ensembl
Innerchr15:94785013..94786136hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381124
hg191124
hg181124
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974621
Supporting Variants
SamplesHGDP00542
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)nssv2037822
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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