A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433043



Internal ID22490913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20667651..20669742hg38UCSC Ensembl
chr7:20707274..20709365hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382092
hg192092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918548
Supporting Variants
Samples
Known GenesABCB5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433043
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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