A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422732



Internal ID21080285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64726920..64727546hg38UCSC Ensembl
chr8:65639477..65640103hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169468
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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