A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895963



Internal ID6302974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102767117..102813354hg19UCSC Ensembl
Outerchr10:102750783..102824292hg19UCSC Ensembl
Innerchr10:102757107..102803344hg18UCSC Ensembl
Outerchr10:102740773..102814282hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1585918
SamplesIS37646
Known GenesC10orf2, KAZALD1, LZTS2, PDZD7, SFXN3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895963
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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