A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013456



Internal ID19102674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87146758..87747090hg38UCSC Ensembl
Innerchr2:87373881..88046609hg19UCSC Ensembl
Innerchr2:87227392..87827724hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38600333
hg19672729
hg18600333
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3901n100
Supporting Variantsnssv3582325, nssv3728764, nssv3582324
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)nsv1013456
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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