A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828763



Internal ID22603698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180754196..180762808hg38UCSC Ensembl
chr1:180723332..180731944hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg388613
hg198613
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451562
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828763
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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