A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421790



Internal ID21079343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62227455..62480058hg38UCSC Ensembl
chr8:63140014..63392617hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38252604
hg19252604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168603
Samples
Known GenesNKAIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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