A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586599



Internal ID21535153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88892389..88893859hg38UCSC Ensembl
chr15:89435620..89437090hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381471
hg191471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095284
SamplesNA20847
Known GenesHAPLN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586599
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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