A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895372



Internal ID6302383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49585567..49931149hg19UCSC Ensembl
Outerchr10:49576878..49933488hg19UCSC Ensembl
Innerchr10:49255573..49601155hg18UCSC Ensembl
Outerchr10:49246884..49603494hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1518269
SamplesSP57481
Known GenesARHGAP22, MAPK8, WDFY4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895372
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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