A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053015



Internal ID20620055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151071741..151084716hg38UCSC Ensembl
chr1:151044217..151057192hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3812976
hg1912976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332733
Supporting Variants
Samples
Known GenesGABPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125


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