A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275994



Internal ID20843034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44688131..44688692hg38UCSC Ensembl
chr7:44727730..44728291hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556891
Supporting Variants
Samples
Known GenesOGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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