A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392212



Internal ID21049765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105815189..105815506hg38UCSC Ensembl
chr4:106736346..106736663hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107021
Samples
Known GenesGSTCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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