A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508757



Internal ID20882061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50408234..50408528hg38UCSC Ensembl
chr15:50700431..50700725hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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