A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142304



Internal ID341504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93936022..93936094hg38UCSC Ensembl
chr8:94948250..94948322hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142304
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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