A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829403



Internal ID22604338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234902051..234904050hg38UCSC Ensembl
chr1:235037798..235039797hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829403
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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