A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014745



Internal ID18757280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87117603..87652179hg38UCSC Ensembl
Innerchr2:87344726..87951698hg19UCSC Ensembl
Innerchr2:87198237..87732813hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38534577
hg19606973
hg18534577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3888n100
Supporting Variantsnssv3582223
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014745
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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