A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384946



Internal ID21042499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89745393..89750062hg38UCSC Ensembl
chr4:90666544..90671213hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg384670
hg194670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122509
Samples
Known GenesSNCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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