A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202445



Internal ID20769485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36405987..36427159hg38UCSC Ensembl
chr1:36871588..36892760hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3821173
hg1921173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329836
Supporting Variants
Samples
Known GenesOSCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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