A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264643



Internal ID20831683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42117983..42118227hg38UCSC Ensembl
chr4:42120000..42120244hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558368
Supporting Variants
Samples
Known GenesBEND4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264643
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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