A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051836



Internal ID20618877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117162085..117180441hg38UCSC Ensembl
chr1:117704707..117723063hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3818357
hg1918357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321527
Supporting Variants
Samples
Known GenesVTCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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