A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428989



Internal ID21086542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68989898..68990328hg38UCSC Ensembl
chr8:69902133..69902563hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170646
Samples
Known GenesLOC100505718
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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