A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516194



Internal ID20889555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12136853..12137273hg38UCSC Ensembl
chr19:12247668..12248088hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044913
Samples
Known GenesZNF20, ZNF625-ZNF20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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