A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560842



Internal ID20933913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39013068..39013541hg38UCSC Ensembl
chr4:39014688..39015161hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5234n223
Supporting Variantsnssv18265124
Samples
Known GenesTMEM156
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560842
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