A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133797



Internal ID20700837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9314773..9315484hg38UCSC Ensembl
chr5:9314885..9315596hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383309
Supporting Variants
Samples
Known GenesSEMA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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