A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316244



Internal ID20849322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20919866..20920027hg38UCSC Ensembl
chr1:21246359..21246520hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057234
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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