A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390445



Internal ID21047998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51993238..51996329hg38UCSC Ensembl
chr4:52859404..52862495hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383092
hg193092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117309
Samples
Known GenesLRRC66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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