A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434526



Internal ID21092079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:2596063..3281914hg38UCSC Ensembl
chr8:2453154..3139436hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38685852
hg19686283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229991
Samples
Known GenesCSMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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