A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389843



Internal ID21047396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169659069..169659667hg38UCSC Ensembl
chr4:170580220..170580818hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115427
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389843
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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