A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951288



Internal ID16953475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:2507371..2541770hg38UCSC Ensembl
Outerchr11:2528601..2563000hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3834400
hg1934400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998130
SamplesBILGI_BIOE
Known GenesKCNQ1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951288
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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