A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18045937



Internal ID20612977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14400776..14402366hg38UCSC Ensembl
chr19:14511588..14513178hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381591
hg191591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516636
Supporting Variants
Samples
Known GenesCD97
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18045937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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