A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379370



Internal ID21036923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99596772..99603184hg38UCSC Ensembl
chr4:100517929..100524341hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg386413
hg196413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121336
Samples
Known GenesMTTP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379370
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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