A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389596



Internal ID22447466
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 StatusS
Merged Variantsnsv5973627
Supporting Variants
Samples
Known GenesSEC14L1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389596
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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