A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384852



Internal ID21042405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176498410..176499162hg38UCSC Ensembl
chr4:177419561..177420313hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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