A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045407



Internal ID21954673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218577199..218577199hg38UCSC Ensembl
chr2:219441922..219441922hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528175
Samples
Known GenesRQCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045407
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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