A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001645



Internal ID68699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113470040..113470775hg38UCSC Ensembl
chr7:113110095..113110830hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001645
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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