A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236844



Internal ID20803884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25422217..25468583hg38UCSC Ensembl
chr8:25279733..25326099hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3846367
hg1946367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430571
Supporting Variants
Samples
Known GenesCDCA2, GNRH1, KCTD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236844
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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