A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532929



Internal ID20906290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38168922..38216472hg38UCSC Ensembl
chr20:36797324..36844874hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3847551
hg1947551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068820
Samples
Known GenesKIAA1755
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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