A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860662



Internal ID22635597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53440972..53448596hg38UCSC Ensembl
chr15:53733169..53740793hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg387625
hg197625
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860662
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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