A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332248



Internal ID20865418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49554501..49564000hg38UCSC Ensembl
chr1:50020173..50029672hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061810
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332248
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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