A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014098



Internal ID18756630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24390678..24497177hg38UCSC Ensembl
Innerchr2:24613547..24720046hg19UCSC Ensembl
Innerchr2:24467051..24573550hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38106500
hg19106500
hg18106500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3727988
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)nsv1014098
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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