A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221259



Internal ID20788299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98806653..99083746hg38UCSC Ensembl
chr7:98404276..98681369hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38277094
hg19277094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616739
Supporting Variants
Samples
Known GenesMIR3609, SMURF1, TMEM130, TRRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221259
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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