A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560977



Internal ID333967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7902322..7902689hg38UCSC Ensembl
chr5:7902435..7902802hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560977
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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