A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080000



Internal ID20647040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1700852..1716347hg38UCSC Ensembl
chr2:1704624..1720119hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3815496
hg1915496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342664
Supporting Variants
Samples
Known GenesPXDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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