A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029834



Internal ID19119053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702933..8751782hg38UCSC Ensembl
Innerchr5:8703045..8751894hg19UCSC Ensembl
Innerchr5:8756045..8804894hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3848850
hg1948850
hg1848850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5564n100
Supporting Variantsnssv3638094
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)nsv1029834
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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