A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959449



Internal ID15906719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14878139..14900108hg38UCSC Ensembl
Innerchr3:14919646..14941615hg19UCSC Ensembl
Innerchr3:14894650..14916619hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3821970
hg1921970
hg1821970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589780
Supporting Variants
Samples
Known GenesFGD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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