A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392123



Internal ID21049676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171273842..171439274hg38UCSC Ensembl
chr4:172194993..172360425hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38165433
hg19165433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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