A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079672



Internal ID21459389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438268..79438340hg38UCSC Ensembl
chr15:79730610..79730682hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591814
Supporting Variants
SamplesHG02818
Known GenesKIAA1024
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079672
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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