A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv912256



Internal ID6274183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49571113..49595007hg19UCSC Ensembl
Outerchr19:49564124..49606449hg19UCSC Ensembl
Innerchr19:54262925..54286819hg18UCSC Ensembl
Outerchr19:54255936..54298261hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1552801
SamplesMS19630
Known GenesKCNA7, NTF4, SNRNP70
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv912256
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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