A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271744



Internal ID20838784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130423058..130424375hg38UCSC Ensembl
chr7:130062899..130064216hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg381318
hg191318
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573831
Supporting Variants
Samples
Known GenesCEP41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271744
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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