A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898638



Internal ID6305649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:6934300..6948899hg19UCSC Ensembl
Outerchr12:6929637..6954864hg19UCSC Ensembl
Innerchr12:6804561..6819160hg18UCSC Ensembl
Outerchr12:6799898..6825125hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1584830
SamplesIS37172
Known GenesCD4, GNB3, GPR162, LEPREL2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898638
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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