A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585281



Internal ID20958352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65757872..65758342hg38UCSC Ensembl
chr15:66050210..66050680hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238912
Samples
Known GenesDENND4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585281
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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