A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457674



Internal ID22515555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97464472..97466697hg38UCSC Ensembl
chr13:98116726..98118951hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg382226
hg192226
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850375
Supporting Variants
Samples
Known GenesRAP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457674
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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