A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146169



Internal ID345374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438123..79439372hg38UCSC Ensembl
chr15:79730465..79731714hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704386
Samples
Known GenesKIAA1024
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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