A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232649



Internal ID20799689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90556333..90592094hg38UCSC Ensembl
chr7:90185647..90221408hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835762
hg1935762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613286
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232649
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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