A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084242



Internal ID21447634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41293509..41293576hg38UCSC Ensembl
chr15:41585707..41585774hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585172
Supporting Variants
SamplesHG00732
Known GenesOIP5-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084242
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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