A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861494



Internal ID22636429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41280519..41282044hg38UCSC Ensembl
chr15:41572717..41574242hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381526
hg191526
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471818, nssv17471819
Samples
Known GenesCHP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861494
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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