A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967660



Internal ID22742595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97579662..98035557hg38UCSC Ensembl
chr2:98196125..98652020hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38455896
hg19455896
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395762
Samples
Known GenesACTR1B, ANKRD36B, COX5B, LINC01125, TMEM131, ZAP70
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967660
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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