A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199891



Internal ID20766931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207340001..207382400hg38UCSC Ensembl
chr1:207513346..207555745hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3842400
hg1942400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318953
Supporting Variants
Samples
Known GenesCD55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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