A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038174



Internal ID93180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112796262..112796279hg38UCSC Ensembl
chr10:114556021..114556038hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538499
Supporting Variants
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038174
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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