A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422546



Internal ID21080099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62897092..62903979hg38UCSC Ensembl
chr8:63809651..63816538hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg386888
hg196888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169778
Samples
Known GenesNKAIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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