A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv892071



Internal ID6299082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2619915..2625353hg19UCSC Ensembl
Outerchr9:2618969..2626031hg19UCSC Ensembl
Innerchr9:2609915..2615353hg18UCSC Ensembl
Outerchr9:2608969..2616031hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1509928
SamplesSP54956
Known GenesFLJ35024, VLDLR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv892071
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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