A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952742



Internal ID16954929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118218486..118228985hg38UCSC Ensembl
Outerchr11:118089201..118099700hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999626
SamplesBILGI_BIOE
Known GenesAMICA1, MPZL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952742
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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