A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078075



Internal ID21987308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32228609..32228609hg38UCSC Ensembl
chr5:32228715..32228715hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537687
Samples
Known GenesMTMR12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078075
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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