A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142419



Internal ID341619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36391345..36410372hg38UCSC Ensembl
chr8:36248863..36267890hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3819028
hg1919028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142419
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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