A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142559



Internal ID341760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105380604..105380928hg38UCSC Ensembl
chr8:106392832..106393156hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016669
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142559
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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