A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973627



Internal ID22748562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77096387..77121348hg38UCSC Ensembl
chr17:75092469..75117430hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3824962
hg1924962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389596
Samples
Known GenesSEC14L1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973627
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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