A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572655



Internal ID20945726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77576002..77576440hg38UCSC Ensembl
chr7:77205319..77205757hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276617
Samples
Known GenesPTPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572655
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