A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016056



Internal ID78352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95507786..95508697hg38UCSC Ensembl
chr8:96520014..96520925hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38912
hg19912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478773
Supporting Variants
Samples
Known GenesLOC100616530
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016056
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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