A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384310



Internal ID21041863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89751290..89751637hg38UCSC Ensembl
chr4:90672441..90672788hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122510
Samples
Known GenesSNCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384310
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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