A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071852



Internal ID21981085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146728815..146728815hg38UCSC Ensembl
chr4:147649967..147649967hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553242
Samples
Known GenesTTC29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071852
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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