A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061774



Internal ID20628814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49368230..49430188hg38UCSC Ensembl
chr1:49833902..49895860hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3861959
hg1961959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317437
Supporting Variants
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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