A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035193



Internal ID19124412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98056829..98412123hg38UCSC Ensembl
Innerchr11:97927557..98282852hg19UCSC Ensembl
Innerchr11:97432767..97788062hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38355295
hg19355296
hg18355296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1260n100
Supporting Variantsnssv3503532
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)nsv1035193
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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