A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386965



Internal ID22444835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67597984..67611731hg38UCSC Ensembl
chr17:65594100..65607847hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3813748
hg1913748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970922
Supporting Variants
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386965
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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