A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828731



Internal ID22603666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172313520..172322558hg38UCSC Ensembl
chr1:172282660..172291698hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg389039
hg199039
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463907
Samples
Known GenesDNM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828731
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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