A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466058



Internal ID22523948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110443765..110445064hg38UCSC Ensembl
chr12:110881570..110882869hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852870
Supporting Variants
Samples
Known GenesARPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466058
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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