A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872533



Internal ID22647473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6662038..6662279hg38UCSC Ensembl
chr1:6722098..6722339hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373499
Samples
Known GenesDNAJC11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872533
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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