A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383188



Internal ID21040741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169007578..169013605hg38UCSC Ensembl
chr4:169928729..169934756hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386028
hg196028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115375
Samples
Known GenesCBR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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