A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046269



Internal ID20613309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35056253..35056696hg38UCSC Ensembl
chr19:35547157..35547600hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529578
Supporting Variants
Samples
Known GenesHPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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