A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266713



Internal ID20833753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87341216..87341605hg38UCSC Ensembl
chr4:88262368..88262757hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573754
Supporting Variants
Samples
Known GenesHSD17B11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266713
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer