A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088702



Internal ID20655742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45219615..45226316hg38UCSC Ensembl
chr2:45446754..45453455hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg386702
hg196702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342589
Supporting Variants
Samples
Known GenesLINC01121
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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