A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472309



Internal ID22530201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75296833..75301781hg38UCSC Ensembl
chr15:75589174..75594122hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg384949
hg194949
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859684
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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