A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434152



Internal ID21091705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54373734..54375540hg38UCSC Ensembl
chr8:55286294..55288100hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381807
hg191807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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