A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968909



Internal ID22743844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184990077..186324974hg38UCSC Ensembl
chr4:185911231..187246128hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381334898
hg191334898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425415
Samples
Known GenesANKRD37, C4orf47, CCDC110, CYP4V2, F11, F11-AS1, FAM149A, FLJ38576, HELT, KIAA1430, KLKB1, LRP2BP, PDLIM3, SLC25A4, SNX25, SORBS2, TLR3, UFSP2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968909
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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