A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096056



Internal ID20663096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15334501..15340698hg38UCSC Ensembl
chr3:15376008..15382205hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386198
hg196198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359201
Supporting Variants
Samples
Known GenesSH3BP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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