A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203183



Internal ID20770223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93291706..93316742hg38UCSC Ensembl
chr1:93757263..93782299hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3825037
hg1925037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335114
Supporting Variants
Samples
Known GenesLOC100131564
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203183
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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