A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112657



Internal ID20679697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165608301..165614400hg38UCSC Ensembl
chr4:166529453..166535552hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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