A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430215



Internal ID21087768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:3538616..3567209hg38UCSC Ensembl
chr8:3396138..3424731hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg3828594
hg1928594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167403
Samples
Known GenesCSMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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