A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071555



Internal ID21980788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90094497..90094497hg38UCSC Ensembl
chr6:90804216..90804216hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383413
hg193413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568137
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071555
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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