A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141704



Internal ID340901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42082077..42090990hg38UCSC Ensembl
chr8:41939595..41948508hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388914
hg198914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141704
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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