A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424642



Internal ID21082195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21276100..21574774hg38UCSC Ensembl
chr9:21276099..21574773hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38298675
hg19298675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230335
Samples
Known GenesIFNA1, IFNA13, IFNA2, IFNA22P, IFNA5, IFNA6, IFNA8, IFNE, KLHL9, MIR31, MIR31HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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