A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029641



Internal ID19118859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29861031..29940764hg38UCSC Ensembl
Innerchr5:29861138..29940871hg19UCSC Ensembl
Innerchr5:29896895..29976628hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3879734
hg1979734
hg1879734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5616n100
Supporting Variantsnssv3745866
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)nsv1029641
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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