A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504886



Internal ID20878150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55416226..55419041hg38UCSC Ensembl
chr15:55708424..55711239hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382816
hg192816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024838
Samples
Known GenesC15orf65, DYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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