A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048342



Internal ID20615382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4803438..4807025hg38UCSC Ensembl
chr19:4803450..4807037hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383588
hg193588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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