A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040561



Internal ID19129780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54782034..54852259hg38UCSC Ensembl
Innerchr11:51267021..51337246hg19UCSC Ensembl
Innerchr11:51123597..51193822hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3870226
hg1970226
hg1870226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1156n100
Supporting Variantsnssv3507769
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)nsv1040561
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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