A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105078



Internal ID20672118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106662801..106663700hg38UCSC Ensembl
chr4:107583958..107584857hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377971
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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