A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18088828



Internal ID20655868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68301765..68321592hg38UCSC Ensembl
chr2:68528897..68548724hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3819828
hg1919828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347524
Supporting Variants
Samples
Known GenesCNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18088828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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