A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592297



Internal ID20965368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49525542..49525931hg38UCSC Ensembl
chr13:50099678..50100067hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222863
Samples
Known GenesPHF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592297
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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