A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103654



Internal ID22012888
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 StatusM
Merged Variants
Supporting Variantsnssv17528601
Samples
Known GenesDNTTIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103654
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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