A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000488



Internal ID67903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98327299..98335091hg38UCSC Ensembl
chr7:97956611..97964403hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg387793
hg197793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493489
Supporting Variants
Samples
Known GenesBAIAP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000488
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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