A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106839



Internal ID20673879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100531790..100532496hg38UCSC Ensembl
chr4:101452947..101453653hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106839
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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