A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046583



Internal ID19135802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97134778..97237386hg38UCSC Ensembl
Innerchr11:97005778..97108386hg19UCSC Ensembl
Innerchr11:96510988..96613596hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38102609
hg19102609
hg18102609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1258n100
Supporting Variantsnssv3505262, nssv3510623
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)nsv1046583
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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