A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725101



Internal ID148767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42048477..42050610hg38UCSC Ensembl
chr19:42552629..42554762hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382134
hg192134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518849
Supporting Variants
Samples
Known GenesGRIK5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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