A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200357



Internal ID20767397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119030001..119036300hg38UCSC Ensembl
chr1:119572624..119578923hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321958
Supporting Variants
Samples
Known GenesWARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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