A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516578



Internal ID20889939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32707773..32816786hg38UCSC Ensembl
chr19:33198679..33307692hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38109014
hg19109014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047673
Samples
Known GenesNUDT19, TDRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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