A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539573



Internal ID20912869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153415136..153461948hg38UCSC Ensembl
chr1:153387612..153434424hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3846813
hg1946813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv386n223
Supporting Variantsnssv18247046
Samples
Known GenesS100A7, S100A7A, S100A7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539573
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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