A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276628



Internal ID20843668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77637805..77638221hg38UCSC Ensembl
chr7:77267122..77267538hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562417
Supporting Variants
Samples
Known GenesPTPN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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