A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565631



Internal ID20938702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43571774..43572215hg38UCSC Ensembl
chr6:43539511..43539952hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271357
Samples
Known GenesXPO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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