A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2018611



Internal ID17769419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34941924..34943980hg38UCSC Ensembl
Innerchr15:35234125..35236181hg19UCSC Ensembl
Innerchr15:33021417..33023473hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382057
hg192057
hg182057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977699
Supporting Variants
SamplesHGDP00542
Known GenesAQR
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)nssv2018611
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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