A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098612



Internal ID20665652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21379860..21418344hg38UCSC Ensembl
chr3:21421352..21459836hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3838485
hg1938485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359257
Supporting Variants
Samples
Known GenesVENTXP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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