A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276642



Internal ID20843682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77744608..77745000hg38UCSC Ensembl
chr7:77373925..77374317hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567876
Supporting Variants
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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