A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135612



Internal ID20702653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95636329..95655196hg38UCSC Ensembl
chr5:94972033..94990900hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3818868
hg1918868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409343
Supporting Variants
Samples
Known GenesRFESD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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