A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104157



Internal ID20671197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87151901..87156800hg38UCSC Ensembl
chr3:87201051..87205950hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368234
Supporting Variants
Samples
Known GenesLINC00506
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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