A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584843



Internal ID20957914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51382007..51382877hg38UCSC Ensembl
chr13:51956143..51957013hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226850
Samples
Known GenesINTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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