A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv881270



Internal ID6288281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:175414234..175424172hg19UCSC Ensembl
Outerchr4:175413296..175425619hg19UCSC Ensembl
Innerchr4:175650809..175660747hg18UCSC Ensembl
Outerchr4:175649871..175662194hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1505264
SamplesSP53347
Known GenesHPGD
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv881270
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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