A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047596



Internal ID20614636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3854105..3859748hg38UCSC Ensembl
chr19:3854103..3859746hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385644
hg195644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530737
Supporting Variants
Samples
Known GenesZFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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