A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046322



Internal ID19135541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107460595..107476508hg38UCSC Ensembl
Innerchr11:107331321..107347234hg19UCSC Ensembl
Innerchr11:106836531..106852444hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3815914
hg1915914
hg1815914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1273n100
Supporting Variantsnssv3518017, nssv3520082, nssv3509013, nssv3502773
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)nsv1046322
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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