A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006976



Internal ID19096194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89408107..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg18550584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3965n100
Supporting Variantsnssv3579783, nssv3730087, nssv3730093, nssv3730088, nssv3730090, nssv3579782, nssv3579781, nssv3730091, nssv3730092, nssv3730089
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006976
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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