A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219352



Internal ID20786392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8009435..8025453hg38UCSC Ensembl
chr7:8049065..8065083hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3816019
hg1916019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617633
Supporting Variants
Samples
Known GenesGLCCI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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