A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579606



Internal ID20952677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63933938..63936596hg38UCSC Ensembl
chr15:64226137..64228795hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382659
hg192659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238796
Samples
Known GenesDAPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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