A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981768



Internal ID21891111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174833865..174850091hg38UCSC Ensembl
chr1:174803003..174819229hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3816227
hg1916227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518094
Samples
Known GenesRABGAP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981768
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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