A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506385



Internal ID20879664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55483813..55486451hg38UCSC Ensembl
chr15:55776011..55778649hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382639
hg192639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024845
Samples
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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