A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471812



Internal ID22529704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40656237..40666303hg38UCSC Ensembl
chr15:40948435..40958501hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810067
hg1910067
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851769
Supporting Variants
Samples
Known GenesCASC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471812
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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