A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276621



Internal ID20843661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77624215..77624556hg38UCSC Ensembl
chr7:77253532..77253873hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567140
Supporting Variants
Samples
Known GenesPTPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276621
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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