A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039861



Internal ID19129080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60174137..60238144hg38UCSC Ensembl
Innerchr15:60466336..60530343hg19UCSC Ensembl
Innerchr15:58253628..58317635hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3864008
hg1964008
hg1864008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2610n100
Supporting Variantsnssv3553619
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)nsv1039861
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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