A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008106



Internal ID19097325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22289612..22383088hg38UCSC Ensembl
Innerchr2:22512484..22605960hg19UCSC Ensembl
Innerchr2:22365989..22459465hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3893477
hg1993477
hg1893477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3727962
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008106
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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