A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859884



Internal ID22043527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151823472..151823472hg38UCSC Ensembl
chr6:152144607..152144607hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257354
Supporting Variants
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859884
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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