A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505232



Internal ID20878499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21423371..21709240hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38285870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3035n223
Supporting Variantsnssv18034307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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