A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352851



Internal ID22578520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24952189..24957813hg38UCSC Ensembl
chr10:25241118..25246742hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385625
hg195625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969430
Supporting Variants
Samples
Known GenesPRTFDC1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352851
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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