A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv901049



Internal ID6262976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113659108..114085804hg19UCSC Ensembl
Outerchr13:113647190..114088843hg19UCSC Ensembl
Innerchr13:112707109..113133805hg18UCSC Ensembl
Outerchr13:112695191..113136844hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546842
SamplesMS17208
Known GenesADPRHL1, CUL4A, F10, F7, GRTP1, LAMP1, MCF2L, PCID2, PROZ
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv901049
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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