A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071328



Internal ID21980561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153585245..153585245hg38UCSC Ensembl
chr5:152964805..152964805hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561123
Samples
Known GenesGRIA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071328
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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