A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471795



Internal ID22529687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38007742..38032901hg38UCSC Ensembl
chr15:38299943..38325102hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3825160
hg1925160
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471795
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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