A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142107



Internal ID19265135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:33625953..33648591hg38UCSC Ensembl
Outerchr11:33647499..33670137hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3822639
hg1922639
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962251, nssv3983699
SamplesKWS2, KWS1
Known GenesKIAA1549L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142107
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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