A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257359



Internal ID22061969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151960111..151960111hg38UCSC Ensembl
chr6:152281246..152281246hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859889
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257359
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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