A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379680



Internal ID21037233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176355484..176359004hg38UCSC Ensembl
chr4:177276635..177280155hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg383521
hg193521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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