A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001110



Internal ID19090327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149856055..149877896hg38UCSC Ensembl
Innerchr2:150712569..150734410hg19UCSC Ensembl
Innerchr2:150420815..150442656hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3821842
hg1921842
hg1821842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582961
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)nsv1001110
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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