A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323919



Internal ID20857042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49454801..49455700hg38UCSC Ensembl
chr1:49920473..49921372hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061791
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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