A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223814



Internal ID20790854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135749027..135793307hg38UCSC Ensembl
chr7:135433775..135478055hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3844281
hg1944281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435292
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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