A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124584



Internal ID20691624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:125118270..125171893hg38UCSC Ensembl
chr5:124453963..124507586hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3853624
hg1953624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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