A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv899089



Internal ID6306100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52675098..52777513hg19UCSC Ensembl
Outerchr12:52666920..52782141hg19UCSC Ensembl
Innerchr12:50961365..51063780hg18UCSC Ensembl
Outerchr12:50953187..51068408hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1585953
SamplesIS37646
Known GenesKRT81, KRT83, KRT84, KRT85, KRT86
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv899089
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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