A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv879683



Internal ID6286694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103807720..103887561hg19UCSC Ensembl
Outerchr4:103785051..103916717hg19UCSC Ensembl
Innerchr4:104027155..104107010hg18UCSC Ensembl
Outerchr4:104004140..104136166hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1594123
SamplesIS39716
Known GenesCISD2, SLC9B1, UBE2D3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv879683
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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