A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051685



Internal ID20618725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115049868..115050450hg38UCSC Ensembl
chr1:115592489..115593071hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334844
Supporting Variants
Samples
Known GenesTSPAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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