A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829252



Internal ID22604187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235346453..235349152hg38UCSC Ensembl
chr1:235509768..235512467hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829252
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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