A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001174



Internal ID68369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78273099..78290094hg38UCSC Ensembl
chr7:77902416..77919411hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3816996
hg1916996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147104
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001174
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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