A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17015719



Internal ID78128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101623343..101623867hg38UCSC Ensembl
chr8:102635571..102636095hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492751
Supporting Variants
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17015719
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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