A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080280



Internal ID20647320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16706875..16707756hg38UCSC Ensembl
chr2:16888142..16889023hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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