A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379991



Internal ID21037544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127912919..127914417hg38UCSC Ensembl
chr4:128834074..128835572hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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