A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040669



Internal ID19129888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93682592..93779442hg38UCSC Ensembl
Innerchr15:94225821..94322671hg19UCSC Ensembl
Innerchr15:92026825..92123675hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3896851
hg1996851
hg1896851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718209
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)nsv1040669
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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