A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119445



Internal ID20686485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67086261..67124454hg38UCSC Ensembl
chr4:67951979..67990172hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3838194
hg1938194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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