A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894125



Internal ID22669194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157847066..157917746hg38UCSC Ensembl
chr5:157274074..157344754hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3870681
hg1970681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427157
Samples
Known GenesCLINT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894125
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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