A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995502



Internal ID64441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44616726..44616826hg38UCSC Ensembl
chr7:44656325..44656425hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147282
Supporting Variants
Samples
Known GenesOGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995502
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.012492


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