A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141462



Internal ID340658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78669386..78669462hg38UCSC Ensembl
chr8:79581621..79581697hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012940
Samples
Known GenesZC2HC1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141462
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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