A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721335



Internal ID145001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10564028..10564342hg38UCSC Ensembl
chr19:10674704..10675018hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519822
Supporting Variants
Samples
Known GenesKRI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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