A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151885



Internal ID15534484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14868122..14906032hg38UCSC Ensembl
Innerchr3:14909629..14947539hg19UCSC Ensembl
Innerchr3:14884633..14922543hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3837911
hg1937911
hg1837911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589779
Supporting Variants
SamplesNINDS_78
Known GenesFGD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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