A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862436



Internal ID22637371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44956025..44964895hg38UCSC Ensembl
chr15:45248223..45257093hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388871
hg198871
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471900
Samples
Known GenesC15orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862436
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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