A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011527



Internal ID18754061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87023361..87752799hg38UCSC Ensembl
Innerchr2:87250484..88052318hg19UCSC Ensembl
Innerchr2:87103995..87833433hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38729439
hg19801835
hg18729439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3888n100
Supporting Variantsnssv3728716, nssv3582176
Samples
Known GenesLINC00152, LOC285074, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2, PLGLB1, PLGLB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011527
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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