A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417131



Internal ID21074684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85117296..85117941hg38UCSC Ensembl
chr8:86029531..86030176hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172038
Samples
Known GenesLRRCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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