A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735858



Internal ID159524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123213745..123218556hg38UCSC Ensembl
chr8:124225985..124230796hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg384812
hg194812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486310
Supporting Variants
Samples
Known GenesMIR4663
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735858
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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