A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202824



Internal ID20769864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25147588..25148091hg38UCSC Ensembl
chr1:25474079..25474582hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329248
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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