A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103315



Internal ID22012548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26661917..26661917hg38UCSC Ensembl
chr22:27057881..27057881hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649117
Samples
Known GenesMIAT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103315
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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