A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210689



Internal ID20777729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:91437401..91505700hg38UCSC Ensembl
chr2:90408470..90481169hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3868300
hg1972700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355310
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.49039


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