A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601153



Internal ID21549797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81323239..81323316hg38UCSC Ensembl
chr15:81615580..81615657hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088208
SamplesHG00513
Known GenesSTARD5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601153
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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