A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053770



Internal ID20620810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176930193..176931681hg38UCSC Ensembl
chr1:176899329..176900817hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381489
hg191489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318495
Supporting Variants
Samples
Known GenesASTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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