A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070616



Internal ID21979849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174320699..174320699hg38UCSC Ensembl
chr4:175241850..175241850hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546447
Samples
Known GenesCEP44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070616
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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