A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv883074



Internal ID6290085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160312017..162000454hg19UCSC Ensembl
Outerchr5:160296233..162011959hg19UCSC Ensembl
Innerchr5:160244595..161933032hg18UCSC Ensembl
Outerchr5:160228811..161944537hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1556156
SamplesMS21840
Known GenesGABRA1, GABRA6, GABRB2, GABRG2, LOC285629
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv883074
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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