A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280666



Internal ID20847706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37160884..37161189hg38UCSC Ensembl
chr9:37160881..37161186hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562973
Supporting Variants
Samples
Known GenesZCCHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280666
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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