A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496420



Internal ID20869622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37656387..37732021hg38UCSC Ensembl
chr15:37948588..38024222hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3875635
hg1975635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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