A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828659



Internal ID22603594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178761240..178763239hg38UCSC Ensembl
chr1:178730375..178732374hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463475
Samples
Known GenesRALGPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828659
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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