A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv899868



Internal ID6306879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20674044..20725636hg19UCSC Ensembl
Outerchr13:20664819..20733403hg19UCSC Ensembl
Innerchr13:19572044..19623636hg18UCSC Ensembl
Outerchr13:19562819..19631403hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1544193
SamplesMS16309
Known GenesGJA3, ZMYM2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv899868
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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