A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2038178



Internal ID17754572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93061784..93063421hg38UCSC Ensembl
Innerchr15:93605013..93606650hg19UCSC Ensembl
Innerchr15:91406017..91407654hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381638
hg191638
hg181638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv976965
Supporting Variants
SamplesHGDP00521
Known GenesRGMA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2038178
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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