A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472888



Internal ID22530780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54055727..54058787hg38UCSC Ensembl
chr15:54347924..54350984hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383061
hg193061
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866948
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472888
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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