A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874328



Internal ID22649280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20606063..20607306hg38UCSC Ensembl
chr1:20932556..20933799hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381244
hg191244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368946
Samples
Known GenesCDA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874328
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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