A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv892073



Internal ID6299084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2621030..2627020hg19UCSC Ensembl
Outerchr9:2620592..2627365hg19UCSC Ensembl
Innerchr9:2611030..2617020hg18UCSC Ensembl
Outerchr9:2610592..2617365hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1503559
SamplesSP52077
Known GenesFLJ35024, VLDLR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv892073
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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