A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427699



Internal ID21085252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90975604..90976247hg38UCSC Ensembl
chr8:91987832..91988475hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172730
Samples
Known GenesC8orf88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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