A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144571



Internal ID18919012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:59783010..59783077hg38UCSC Ensembl
Outerchr11:59550483..59550550hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995408
SamplesKWS1
Known GenesSTX3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144571
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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