A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388599



Internal ID21046152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86934801..86935200hg38UCSC Ensembl
chr4:87855953..87856352hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121754
Samples
Known GenesAFF1, LOC100506746
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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