A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382764



Internal ID21040317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145803569..145804649hg38UCSC Ensembl
chr4:146724721..146725801hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108903
Samples
Known GenesZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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