A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227182



Internal ID20794222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158441201..158595200hg38UCSC Ensembl
chr7:158233893..158387892hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38154000
hg19154000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426532
Supporting Variants
Samples
Known GenesMIR5707, MIR595, PTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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