A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393668



Internal ID21051221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233611..40235439hg38UCSC Ensembl
chr4:40235231..40237059hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381829
hg191829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117094
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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