A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085664



Internal ID20652704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26598082..26604413hg38UCSC Ensembl
chr2:26820950..26827281hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg386332
hg196332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336462
Supporting Variants
Samples
Known GenesCIB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085664
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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