A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502099



Internal ID20875340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95009201..95192600hg38UCSC Ensembl
chr15:95552430..95735829hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38183400
hg19183400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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