A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767654



Internal ID20543514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37901687..37901687hg38UCSC Ensembl
chr4:37903308..37903308hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263446
Samples
Known GenesTBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767654
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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