A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051021



Internal ID18793552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49670632..50699606hg38UCSC Ensembl
Innerchr11:49692184..50658777hg19UCSC Ensembl
Innerchr11:49648760..50615353hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381028975
hg19966594
hg18966594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1128n100
Supporting Variantsnssv3513480
Samples
Known GenesLOC440040, LOC441601, LOC646813, OR4C12, OR4C13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051021
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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