A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108968



Internal ID20676008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121365601..121368800hg38UCSC Ensembl
chr4:122286756..122289955hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388416
Supporting Variants
Samples
Known GenesQRFPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01478


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