A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863885



Internal ID22638820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37318528..37321128hg38UCSC Ensembl
chr15:37610729..37613329hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382601
hg192601
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471793, nssv17471792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863885
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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