A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079733



Internal ID21469659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30733798..30733877hg38UCSC Ensembl
chr13:31307935..31308014hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586581
Supporting Variants
SamplesHG03125
Known GenesALOX5AP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079733
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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