A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107788



Internal ID20674828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110018402..110022311hg38UCSC Ensembl
chr4:110939558..110943467hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383910
hg193910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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