A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034497



Internal ID90698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45838765..45958265hg38UCSC Ensembl
chr10:46334213..46426964hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38119501
hg1992752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476203
Supporting Variants
Samples
Known GenesAGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034497
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009256


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