A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120240



Internal ID20687280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75939146..75941557hg38UCSC Ensembl
chr4:76860299..76862710hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382412
hg192412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390775
Supporting Variants
Samples
Known GenesNAAA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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