A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141685



Internal ID340882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62249738..62317000hg38UCSC Ensembl
chr9:46561040..46628301hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3867263
hg1967262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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