A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121437



Internal ID20688477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96862601..96869200hg38UCSC Ensembl
chr4:97783752..97790351hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00384


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