A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135603



Internal ID20702644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95513965..95514590hg38UCSC Ensembl
chr5:94849669..94850294hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410404
Supporting Variants
Samples
Known GenesTTC37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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