A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828520



Internal ID22603455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166944049..166945262hg38UCSC Ensembl
chr1:166913286..166914499hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452784
Samples
Known GenesILDR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828520
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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