A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418692



Internal ID21076245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76491112..76501084hg38UCSC Ensembl
chr8:77403347..77413319hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg389973
hg199973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171356
Samples
Known GenesLINC01111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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