A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381889



Internal ID21039442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174463847..174464489hg38UCSC Ensembl
chr4:175384998..175385640hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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