A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471012



Internal ID22528903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23746913..23750360hg38UCSC Ensembl
chr15:23992060..23995507hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383448
hg193448
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855182
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471012
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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