A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2019168



Internal ID17440144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41556020..41558048hg38UCSC Ensembl
Innerchr15:41848218..41850246hg19UCSC Ensembl
Innerchr15:39635510..39637538hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382029
hg192029
hg182029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984058
Supporting Variants
SamplesHGDP00665
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)nssv2019168
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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