A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv886797



Internal ID6293808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158552774..158756832hg19UCSC Ensembl
Outerchr6:158523142..158764191hg19UCSC Ensembl
Innerchr6:158472762..158676820hg18UCSC Ensembl
Outerchr6:158443130..158684179hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1599893
SamplesIS41806
Known GenesGTF2H5, SERAC1, TULP4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv886797
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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