A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276535



Internal ID20843575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74689715..74690188hg38UCSC Ensembl
chr7:74104049..74104522hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575330
Supporting Variants
Samples
Known GenesGTF2I
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276535
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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