A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561243



Internal ID20934314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43196352..43197005hg38UCSC Ensembl
chr5:43196454..43197107hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268391
Samples
Known GenesNIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561243
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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