A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880612



Internal ID22655582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236038674..236038843hg38UCSC Ensembl
chr1:236201974..236202143hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367705
Samples
Known GenesNID1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880612
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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