A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736174



Internal ID20512121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151847203..151847259hg38UCSC Ensembl
chr1:151819679..151819735hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293771
Samples
Known GenesTHEM5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736174
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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