A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333489



Internal ID20866666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40511089..40516360hg38UCSC Ensembl
chr1:40976761..40982032hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg385272
hg195272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060758
Samples
Known GenesEXO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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