A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738624



Internal ID20514594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111414884..111414953hg38UCSC Ensembl
chr1:111957506..111957575hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275503
Samples
Known GenesOVGP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738624
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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