A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028953



Internal ID87004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6107863..6107914hg38UCSC Ensembl
chr10:6149826..6149877hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5397312
Supporting Variants
Samples
Known GenesRBM17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028953
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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