A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212267



Internal ID20779307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56203306..56228929hg38UCSC Ensembl
chr3:56237334..56262957hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3825624
hg1925624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373449
Supporting Variants
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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