A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074676



Internal ID20641716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100567590..100578559hg38UCSC Ensembl
chr2:101184052..101195021hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3810970
hg1910970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343808
Supporting Variants
Samples
Known GenesPDCL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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