A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601243



Internal ID21549887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81385313..81385588hg38UCSC Ensembl
chr15:81677654..81677929hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080324
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601243
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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