A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564700



Internal ID20937771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23314942..23316678hg38UCSC Ensembl
chr7:23354561..23356297hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272688
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564700
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