A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067526



Internal ID21976759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14960257..14960257hg38UCSC Ensembl
chr4:14961881..14961881hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554632
Samples
Known GenesCPEB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067526
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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