A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048271



Internal ID21957504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9478577..9478577hg38UCSC Ensembl
chr2:9618706..9618706hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522265
Samples
Known GenesIAH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048271
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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