A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571624



Internal ID20944695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140362302..141000082hg38UCSC Ensembl
chr4:141283456..141921236hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38637781
hg19637781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5478n223
Supporting Variantsnssv18264722
Samples
Known GenesCLGN, ELMOD2, LOC100129858, LOC152586, RNF150, SCOC, TBC1D9, TNRC18P1, UCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571624
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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