A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804568



Internal ID21249906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12810912..12810912hg38UCSC Ensembl
chr4:49168251..49168251hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804568
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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