A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207147



Internal ID20774188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87634601..87644800hg38UCSC Ensembl
chr2:87934120..87944319hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01062


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