A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381912



Internal ID21039465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84153267..84153841hg38UCSC Ensembl
chr4:85074420..85074994hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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