A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434392



Internal ID21091945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113876556..113877725hg38UCSC Ensembl
chr8:114888785..114889954hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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