A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232363



Internal ID20799403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90318201..90327200hg38UCSC Ensembl
chr7:89947515..89956514hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232363
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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