A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037403



Internal ID19126622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49998018..50792187hg38UCSC Ensembl
Innerchr11:50019556..50751358hg19UCSC Ensembl
Innerchr11:49976132..50707934hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38794170
hg19731803
hg18731803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1134n100
Supporting Variantsnssv3712371
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037403
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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