A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379246



Internal ID21036799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112460361..112463463hg38UCSC Ensembl
chr4:113381517..113384619hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383103
hg193103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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