A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv875744



Internal ID6282755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208957750..208991487hg19UCSC Ensembl
Outerchr2:208952810..208994045hg19UCSC Ensembl
Innerchr2:208665995..208699732hg18UCSC Ensembl
Outerchr2:208661055..208702290hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1574107
SamplesIS33514
Known GenesCRYGC, CRYGD, LOC100507443
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv875744
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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