A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113525



Internal ID20680565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171286501..171288100hg38UCSC Ensembl
chr4:172207652..172209251hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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