A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472394



Internal ID22530286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91727321..91728820hg38UCSC Ensembl
chr15:92270551..92272050hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472394
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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