A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999995



Internal ID67576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73467107..73467588hg38UCSC Ensembl
chr7:72881437..72881918hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474248
Supporting Variants
Samples
Known GenesBAZ1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999995
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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