A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124633



Internal ID18934446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:104000..196800hg38UCSC Ensembl
Outerchr11:104000..196800hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3892801
hg1992801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976688
SamplesKWS2
Known GenesLINC01001, LOC653486, ODF3, SCGB1C1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124633
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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