A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751987



Internal ID20527847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7863672..7863672hg38UCSC Ensembl
chr10:7905635..7905635hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293665
Samples
Known GenesTAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751987
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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