A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078795



Internal ID20645835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14810455..14811761hg38UCSC Ensembl
chr2:14950579..14951885hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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