A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395314



Internal ID21052867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135392751..135528987hg38UCSC Ensembl
chr4:136313906..136450142hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38136237
hg19136237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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