A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529474



Internal ID20902835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37468708..37525675hg38UCSC Ensembl
chr19:37959610..38016577hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3856968
hg1956968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046651
Samples
Known GenesZNF570, ZNF793
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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