A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333341



Internal ID20866517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57804335..57807390hg38UCSC Ensembl
chr1:58270007..58273062hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg383056
hg193056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061873
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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