A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107775



Internal ID20674815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109804925..109806526hg38UCSC Ensembl
chr4:110726081..110727682hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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