A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011417



Internal ID19100634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87321364..87747090hg38UCSC Ensembl
Innerchr2:87548487..88046609hg19UCSC Ensembl
Innerchr2:87401998..87827724hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38425727
hg19498123
hg18425727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3908n100
Supporting Variantsnssv3582436
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011417
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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