A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200374



Internal ID20767414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119647201..119648800hg38UCSC Ensembl
chr1:120189824..120191423hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324873
Supporting Variants
Samples
Known GenesZNF697
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200374
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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