A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264626



Internal ID20831666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41695372..41695460hg38UCSC Ensembl
chr4:41697389..41697477hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567011
Supporting Variants
Samples
Known GenesLIMCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264626
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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