A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029329



Internal ID19118548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29778109..29804895hg38UCSC Ensembl
Innerchr5:29778216..29805002hg19UCSC Ensembl
Innerchr5:29813973..29840759hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3826787
hg1926787
hg1826787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636000
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)nsv1029329
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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