A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202691



Internal ID20769731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225619335..225624416hg38UCSC Ensembl
chr1:225807037..225812118hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg385082
hg195082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333522
Supporting Variants
Samples
Known GenesENAH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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