A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555680



Internal ID20928751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36438665..36439481hg38UCSC Ensembl
chr6:36406442..36407258hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270713
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555680
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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