A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049499



Internal ID20616539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57767285..57770261hg38UCSC Ensembl
chr19:58278653..58281629hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518820
Supporting Variants
Samples
Known GenesZNF586
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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