A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085638



Internal ID20652678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25985684..25987427hg38UCSC Ensembl
chr2:26208553..26210296hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381744
hg191744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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