A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123558



Internal ID20690598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118555618..118702200hg38UCSC Ensembl
chr5:117891313..118037895hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38146583
hg19146583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401970
Supporting Variants
Samples
Known GenesLOC101927280, LOC102467225
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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