A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065078



Internal ID21974311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138920151..138920151hg38UCSC Ensembl
chr7:138604897..138604897hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567453
Samples
Known GenesKIAA1549
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065078
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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