A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046679



Internal ID20613719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37803728..37881646hg38UCSC Ensembl
chr19:38294368..38372286hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3877919
hg1977919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528876
Supporting Variants
Samples
Known GenesLOC100631378, LOC644554
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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