A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507920



Internal ID20881216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79916101..79920400hg38UCSC Ensembl
chr15:80208443..80212742hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026840
Samples
Known GenesST20, ST20-MTHFS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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