A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141609



Internal ID340806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60247114..60248825hg38UCSC Ensembl
chr8:61159673..61161384hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381712
hg191712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012483
Samples
Known GenesCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141609
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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