A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895964



Internal ID6302975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102755779..102767155hg19UCSC Ensembl
Outerchr10:102753819..102770082hg19UCSC Ensembl
Innerchr10:102745769..102757145hg18UCSC Ensembl
Outerchr10:102743809..102760072hg18UCSC 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 Variantsnssv1508989
SamplesSP54725
Known GenesC10orf2, LZTS2, PDZD7
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895964
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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