A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142294



Internal ID341494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60621000..60668558hg38UCSC Ensembl
chr9_gl000199_random:102442..150000hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3847559
hg1947559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142294
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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