A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057105



Internal ID20624145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206856529..206867470hg38UCSC Ensembl
chr1:207029874..207040815hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3810942
hg1910942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330224
Supporting Variants
Samples
Known GenesIL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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