A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558000



Internal ID331077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91481601..91507939hg38UCSC Ensembl
chr7:91110916..91137254hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3826339
hg1926339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558000
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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