A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470659



Internal ID22528549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100940661..100942160hg38UCSC Ensembl
chr15:101480866..101482365hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877380
Supporting Variants
Samples
Known GenesLRRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470659
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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