A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045886



Internal ID20612926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13928896..13929275hg38UCSC Ensembl
chr19:14039709..14040088hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521394
Supporting Variants
Samples
Known GenesCC2D1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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