A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911295



Internal ID6273222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18875568..18895865hg19UCSC Ensembl
Outerchr19:18874483..18902592hg19UCSC Ensembl
Innerchr19:18736568..18756865hg18UCSC Ensembl
Outerchr19:18735483..18763592hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1511066
SamplesSP54988
Known GenesCOMP, CRTC1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911295
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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