A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233556



Internal ID20800596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122283901..122284900hg38UCSC Ensembl
chr7:121923955..121924954hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233556
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.24836


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