A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384196



Internal ID21041749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154718270..154718879hg38UCSC Ensembl
chr4:155639422..155640031hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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