A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417827



Internal ID22475697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12617103..13191822hg38UCSC Ensembl
chr6:12617335..13192054hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38574720
hg19574720
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977146
Supporting Variants
Samples
Known GenesPHACTR1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417827
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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