A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316930



Internal ID20850012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49785059..49939698hg38UCSC Ensembl
chr1:50250731..50405370hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38154640
hg19154640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061840
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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