A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088904



Internal ID20655944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69861132..69874980hg38UCSC Ensembl
chr2:70088264..70102112hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3813849
hg1913849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337907
Supporting Variants
Samples
Known GenesGMCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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