A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554400



Internal ID16341809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50136389..50776935hg38UCSC Ensembl
Innerchr11:50095560..50736106hg19UCSC Ensembl
Innerchr11:50052136..50692682hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38640547
hg19640547
hg18640547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1815n54
Supporting Variantsnssv773974
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554400
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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