A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062795



Internal ID21972028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151849988..151849988hg38UCSC Ensembl
chr6:152171123..152171123hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570346
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062795
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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