A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394366



Internal ID21051919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52803705..52814864hg38UCSC Ensembl
chr4:53669872..53681031hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3811160
hg1911160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117374
Samples
Known GenesLOC152578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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