A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000000



Internal ID67579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73540688..73540944hg38UCSC Ensembl
chr7:72955018..72955274hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483293
Supporting Variants
Samples
Known GenesBCL7B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000000
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007493


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