A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226599



Internal ID20793639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35898791..35966935hg38UCSC Ensembl
chr7:35938401..36006545hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3868145
hg1968145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609538
Supporting Variants
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226599
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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