A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829996



Internal ID22604931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32776538..32777738hg38UCSC Ensembl
chr1:33242139..33243339hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463624, nssv17468513
Samples
Known GenesYARS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829996
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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