A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144535



Internal ID18909295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12426011..12426066hg38UCSC Ensembl
Outerchr11:12447558..12447613hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995361
SamplesKWS1
Known GenesPARVA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144535
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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