A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155213



Internal ID20722253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13850582..13854818hg38UCSC Ensembl
chr7:13890207..13894443hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg384237
hg194237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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