A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471065



Internal ID22528956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28220849..28225304hg38UCSC Ensembl
chr15:28465995..28470450hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg384456
hg194456
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859302
Supporting Variants
Samples
Known GenesHERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471065
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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