A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274472



Internal ID20841512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140913500..140915065hg38UCSC Ensembl
chr7:140613300..140614865hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567218
Supporting Variants
Samples
Known GenesBRAF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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