A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275237



Internal ID20842277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149482706..149483488hg38UCSC Ensembl
chr7:149179797..149180579hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570634
Supporting Variants
Samples
Known GenesZNF746
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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