A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512974



Internal ID20886314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58813215..58817813hg38UCSC Ensembl
chr15:59105414..59110012hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg384599
hg194599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026198
Samples
Known GenesFAM63B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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