A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026929



Internal ID21936272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438110..79438216hg38UCSC Ensembl
chr15:79730452..79730558hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607583
Samples
Known GenesKIAA1024
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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