A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849334



Internal ID22624269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81125328..81130527hg38UCSC Ensembl
chr15:81417669..81422868hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849334
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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