A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389781



Internal ID21047334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92473770..92589168hg38UCSC Ensembl
chr4:93394921..93510319hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38115399
hg19115399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120748
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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