A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209009



Internal ID20776049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241187272..241254635hg38UCSC Ensembl
chr2:242126687..242194050hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3867364
hg1967364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345721
Supporting Variants
Samples
Known GenesANO7, HDLBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209009
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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