A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv880289



Internal ID6287300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:175413296..175435003hg19UCSC Ensembl
Outerchr4:175412975..175437117hg19UCSC Ensembl
Innerchr4:175649871..175671578hg18UCSC Ensembl
Outerchr4:175649550..175673692hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1503547
SamplesSP52077
Known GenesHPGD
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv880289
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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