A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206571



Internal ID20773611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:121117320..121123850hg38UCSC Ensembl
chr2:121874896..121881426hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg386531
hg196531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206571
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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