A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895716



Internal ID6302727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73509465..73578503hg19UCSC Ensembl
Outerchr10:73507645..73584426hg19UCSC Ensembl
Innerchr10:73179471..73248509hg18UCSC Ensembl
Outerchr10:73177651..73254432hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546738
SamplesMS17208
Known GenesC10orf54, CDH23, PSAP
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895716
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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