A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582615



Internal ID20955686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63789323..63790465hg38UCSC Ensembl
chr17:61866683..61867825hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242627
Samples
Known GenesDDX42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582615
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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