A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv912150



Internal ID6274077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45818527..45827863hg19UCSC Ensembl
Outerchr19:45816547..45830947hg19UCSC Ensembl
Innerchr19:50510367..50519703hg18UCSC Ensembl
Outerchr19:50508387..50522787hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1503585
SamplesSP52077
Known GenesCKM
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv912150
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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