A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510239



Internal ID20883556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51732801..51762600hg38UCSC Ensembl
chr15:52024998..52054797hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3829800
hg1929800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2537n223
Supporting Variantsnssv18182851
Samples
Known GenesLYSMD2, TMOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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