A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265937



Internal ID20832977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70215315..70223108hg38UCSC Ensembl
chr4:71081032..71088825hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg387794
hg197794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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