A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013027



Internal ID19102245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176165949..176196679hg38UCSC Ensembl
Innerchr3:175883737..175914467hg19UCSC Ensembl
Innerchr3:177366431..177397161hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3830731
hg1930731
hg1830731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4988n100
Supporting Variantsnssv3613647, nssv3613645, nssv3738381, nssv3613651, nssv3613652, nssv3738379, nssv3613649, nssv3613644, nssv3738382, nssv3613648, nssv3738380, nssv3613650, nssv3613646
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)nsv1013027
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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