A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266435



Internal ID20833475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55922328..55923038hg38UCSC Ensembl
chr4:56788494..56789204hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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