A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441652



Internal ID22499522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50624389..50630932hg38UCSC Ensembl
chr6:50592102..50598645hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg386544
hg196544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441652
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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