A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109550



Internal ID20676590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147063468..147076192hg38UCSC Ensembl
chr4:147984620..147997344hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3812725
hg1912725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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