A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982829



Internal ID21892172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225784600..225784741hg38UCSC Ensembl
chr1:225972302..225972443hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529083
Samples
Known GenesSRP9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982829
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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