A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142149



Internal ID341349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60560000..60594558hg38UCSC Ensembl
chr9_gl000199_random:41442..76000hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3834559
hg1934559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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