A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999030



Internal ID66921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87502440..87502600hg38UCSC Ensembl
chr7:87131756..87131916hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999030
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.002498


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