A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855182



Internal ID22630117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23746913..23750360hg38UCSC Ensembl
chr15:23992060..23995507hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383448
hg193448
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855182
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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