A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149570



Internal ID20716610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11638618..11643664hg38UCSC Ensembl
chr7:11678245..11683291hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg385047
hg195047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619207
Supporting Variants
Samples
Known GenesTHSD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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