A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221809



Internal ID20788849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158332710..158578397hg38UCSC Ensembl
chr7:158125402..158371089hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38245688
hg19245688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432104
Supporting Variants
Samples
Known GenesMIR595, PTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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