A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377425



Internal ID21034978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51999659..52000319hg38UCSC Ensembl
chr4:52865825..52866485hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117310
Samples
Known GenesLRRC66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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