A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421189



Internal ID22479059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154687391..154966444hg38UCSC Ensembl
chr6:155008525..155287578hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38279054
hg19279054
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972360
Supporting Variants
Samples
Known GenesSCAF8
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421189
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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