A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034704



Internal ID19123925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27324114..27410683hg38UCSC Ensembl
Innerchr5:27324221..27410790hg19UCSC Ensembl
Innerchr5:27359978..27446547hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3886570
hg1986570
hg1886570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5610n100
Supporting Variantsnssv3745861
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)nsv1034704
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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