A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046964



Internal ID20614004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53338603..53393950hg38UCSC Ensembl
chr19:53841856..53897203hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3855348
hg1955348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521155
Supporting Variants
Samples
Known GenesZNF525, ZNF845
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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