A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035092



Internal ID15888278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:73447935..73448642hg38UCSC Ensembl
Innerchr5:72743760..72744467hg19UCSC Ensembl
Innerchr5:72779516..72780223hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38708
hg19708
hg18708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598650
Supporting Variants
Samples
Known GenesFOXD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035092
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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