A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039749



Internal ID19128968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54836089..54886155hg38UCSC Ensembl
Innerchr15:55128287..55178353hg19UCSC Ensembl
Innerchr15:52915579..52965645hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3850067
hg1950067
hg1850067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2603n100
Supporting Variantsnssv3552441
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)nsv1039749
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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