A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089449



Internal ID20656489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60965255..60965881hg38UCSC Ensembl
chr2:61192390..61193016hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341173
Supporting Variants
Samples
Known GenesPUS10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00087


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