A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474942



Internal ID22532837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94435748..94438088hg38UCSC Ensembl
chr15:94978977..94981317hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382341
hg192341
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881404
Supporting Variants
Samples
Known GenesMCTP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474942
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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