A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829929



Internal ID22604864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26211699..26213530hg38UCSC Ensembl
chr1:26538190..26540021hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381832
hg191832
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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