A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227388



Internal ID20794428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149147001..149149000hg38UCSC Ensembl
chr7:148844093..148846092hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417184
Supporting Variants
Samples
Known GenesZNF398
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227388
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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