A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv870975



Internal ID6277986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27113923..27153958hg19UCSC Ensembl
Outerchr1:27112461..27158344hg19UCSC Ensembl
Innerchr1:26986510..27026545hg18UCSC Ensembl
Outerchr1:26985048..27030931hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1509734
SamplesSP54956
Known GenesPIGV, ZDHHC18
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv870975
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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