A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472928



Internal ID22530820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56844114..56848143hg38UCSC Ensembl
chr15:57136312..57140341hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg384030
hg194030
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863202
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472928
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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