A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388828



Internal ID21046381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87264583..87307228hg38UCSC Ensembl
chr4:88185735..88228380hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3842646
hg1942646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121777
Samples
Known GenesHSD17B13, MIR5705
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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