A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567140



Internal ID20940211
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 StatusM
Merged Variants
Supporting Variantsnssv18276621
Samples
Known GenesPTPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567140
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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