A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156909



Internal ID20723949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20667651..20669743hg38UCSC Ensembl
chr7:20707274..20709366hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615745
Supporting Variants
Samples
Known GenesABCB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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