A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145093



Internal ID344298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39747028..39747081hg38UCSC Ensembl
chr15:40039229..40039282hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700089
Samples
Known GenesFSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145093
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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