A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382190



Internal ID21039743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99111307..99116097hg38UCSC Ensembl
chr4:100032458..100037248hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg384791
hg194791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121298
Samples
Known GenesLOC100507053
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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