A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528601



Internal ID21852958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93876138..93882811hg38UCSC Ensembl
chr1:94341694..94348367hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg386674
hg196674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103654
Supporting Variants
Samples
Known GenesDNTTIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528601
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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