A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007268



Internal ID19096487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87229727..87661069hg38UCSC Ensembl
Innerchr2:87456850..87960588hg19UCSC Ensembl
Innerchr2:87310361..87741703hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38431343
hg19503739
hg18431343
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3892n100
Supporting Variantsnssv3582382, nssv3728771, nssv3728772, nssv3728773, nssv3582381
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)nsv1007268
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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