A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515077



Internal ID20888434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52296601..52300000hg38UCSC Ensembl
chr15:52588798..52592197hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515077
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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