A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471900



Internal ID22529792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44956025..44964895hg38UCSC Ensembl
chr15:45248223..45257093hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388871
hg198871
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862436
Supporting Variants
Samples
Known GenesC15orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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