A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975690



Internal ID22750625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27230677..27333214hg38UCSC Ensembl
chr5:27230784..27333321hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38102538
hg19102538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419258
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975690
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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