A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv883305



Internal ID6290316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180493946..180690937hg19UCSC Ensembl
Outerchr5:180493362..180709915hg19UCSC Ensembl
Innerchr5:180426552..180623543hg18UCSC Ensembl
Outerchr5:180425968..180642521hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1576853
SamplesIS34271
Known GenesGNB2L1, MIR4638, OR2V2, SNORD95, SNORD96A, TRIM41, TRIM52, TRIM7
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv883305
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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