A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571712



Internal ID20944783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30780261..30781482hg38UCSC Ensembl
chr4:30781883..30783104hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265069
Samples
Known GenesPCDH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571712
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