A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501653



Internal ID20874890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97420701..97422600hg38UCSC Ensembl
chr15:97963931..97965830hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028615
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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