A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025447



Internal ID18767979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17440462..17642430hg38UCSC Ensembl
Innerchr5:17440571..17642539hg19UCSC Ensembl
Innerchr5:17493571..17675237hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38201969
hg19201969
hg18181667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745745
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025447
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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