A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979280



Internal ID22754215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7902324..7902689hg38UCSC Ensembl
chr5:7902437..7902802hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428603
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979280
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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