A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075908



Internal ID21985141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99588981..99588981hg38UCSC Ensembl
chr4:100510138..100510138hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551082
Samples
Known GenesMTTP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075908
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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