A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379042



Internal ID21036595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169944924..169953410hg38UCSC Ensembl
chr4:170866075..170874561hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg388487
hg198487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115727
Samples
Known GenesLOC100506085
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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