A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765393



Internal ID20541253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151850103..151850103hg38UCSC Ensembl
chr6:152171238..152171238hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260978
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765393
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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