A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418889



Internal ID21076442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69092976..69094336hg38UCSC Ensembl
chr8:70005211..70006571hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170654
Samples
Known GenesLOC100505718
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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