A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209128



Internal ID20776168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26566992..26582698hg38UCSC Ensembl
chr2:26789860..26805566hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3815707
hg1915707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352996
Supporting Variants
Samples
Known GenesC2orf70, CIB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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