A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047490



Internal ID20614530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2969508..2972567hg38UCSC Ensembl
chr19:2969506..2972565hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383060
hg193060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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