A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119566



Internal ID20686606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68730898..68805657hg38UCSC Ensembl
chr4:69596616..69671375hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3874760
hg1974760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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