A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747155



Internal ID20523172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14885255..14885358hg38UCSC Ensembl
chr3:14926762..14926865hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289787
Samples
Known GenesFGD5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747155
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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