A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416725



Internal ID21074278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112458049..112458437hg38UCSC Ensembl
chr8:113470278..113470666hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163563
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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