A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043776



Internal ID19132995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45917646..46061687hg38UCSC Ensembl
Innerchr15:46209844..46353885hg19UCSC Ensembl
Innerchr15:43997136..44141177hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38144042
hg19144042
hg18144042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2591n100
Supporting Variantsnssv3552367
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)nsv1043776
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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