A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv879491



Internal ID6286502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:74276026..74286974hg19UCSC Ensembl
Outerchr4:74275515..74292407hg19UCSC Ensembl
Innerchr4:74494890..74505838hg18UCSC Ensembl
Outerchr4:74494379..74511271hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1505263
SamplesSP53347
Known GenesALB
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv879491
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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