A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829984



Internal ID22604919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30769135..30802326hg38UCSC Ensembl
chr1:31241982..31275173hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3833192
hg1933192
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829984
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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