A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896004



Internal ID6303015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112835109..112839601hg19UCSC Ensembl
Outerchr10:112834763..112842961hg19UCSC Ensembl
Innerchr10:112825099..112829591hg18UCSC Ensembl
Outerchr10:112824753..112832951hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1509082, nssv1510816
SamplesSP54988, SP54750
Known GenesADRA2A
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896004
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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