A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv872533



Internal ID6279544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169490592..169506241hg19UCSC Ensembl
Outerchr1:169490401..169508576hg19UCSC Ensembl
Innerchr1:167757216..167772865hg18UCSC Ensembl
Outerchr1:167757025..167775200hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1503531
SamplesSP52077
Known GenesF5
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv872533
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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