A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863531



Internal ID22638466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38800304..38804603hg38UCSC Ensembl
chr13:39374441..39378740hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461321
Samples
Known GenesFREM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863531
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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