A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110641



Internal ID20677681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127260748..127418136hg38UCSC Ensembl
chr4:128181903..128339291hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38157389
hg19157389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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