A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108481



Internal ID20675521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111496389..111497080hg38UCSC Ensembl
chr4:112417545..112418236hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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