A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829974



Internal ID22604909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28626397..28630045hg38UCSC Ensembl
chr1:28952909..28956557hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383649
hg193649
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465232
Samples
Known GenesTAF12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829974
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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