A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012089



Internal ID19101307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24386584..24404353hg38UCSC Ensembl
Innerchr2:24609453..24627222hg19UCSC Ensembl
Innerchr2:24462957..24480726hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3817770
hg1917770
hg1817770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579128
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)nsv1012089
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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