A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045871



Internal ID21955129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22570496..22570496hg38UCSC Ensembl
chr1:22896989..22896989hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519832
Samples
Known GenesEPHA8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045871
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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