A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572534



Internal ID20945605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37215571..37216092hg38UCSC Ensembl
chr6:37183347..37183868hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270743
Samples
Known GenesTMEM217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572534
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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