A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474917



Internal ID22532812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93244065..93262516hg38UCSC Ensembl
chr15:93787294..93805745hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3818452
hg1918452
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474917
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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