A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333391



Internal ID20866567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49298801..49433700hg38UCSC Ensembl
chr1:49764473..49899372hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38134900
hg19134900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061768
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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