A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967628



Internal ID22742563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77068980..77096472hg38UCSC Ensembl
chr17:75065062..75092554hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3827493
hg1927493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383751
Samples
Known GenesLINC00338, MIR6516, SCARNA16, SEC14L1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967628
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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