A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585033



Internal ID20958104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42845540..42846460hg38UCSC Ensembl
chr15:43137738..43138658hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239025
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585033
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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