A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390499



Internal ID21048052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47856032..47856958hg38UCSC Ensembl
chr4:47858049..47858975hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117249
Samples
Known GenesNFXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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