A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537688



Internal ID20911023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214293697..214294666hg38UCSC Ensembl
chr1:214467040..214468009hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38970
hg19970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248561
Samples
Known GenesSMYD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537688
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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