A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735605



Internal ID20511549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38880089..38880144hg38UCSC Ensembl
chr4:38881710..38881765hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271053
Samples
Known GenesFAM114A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735605
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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