A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403753



Internal ID21061306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84219576..84220115hg38UCSC Ensembl
chr5:83515394..83515933hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135242
Samples
Known GenesEDIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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