A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043521



Internal ID19132740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107688607..107758149hg38UCSC Ensembl
Innerchr11:107559333..107628875hg19UCSC Ensembl
Innerchr11:107064543..107134085hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3869543
hg1969543
hg1869543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1275n100
Supporting Variantsnssv3510034
Samples
Known GenesSLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043521
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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