A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038088



Internal ID19127307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25112285..25272005hg38UCSC Ensembl
Innerchr11:25133831..25293551hg19UCSC Ensembl
Innerchr11:25090407..25250127hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38159721
hg19159721
hg18159721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1077n100
Supporting Variantsnssv3505517, nssv3514925, nssv3508017, nssv3507718, nssv3520752
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)nsv1038088
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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