A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040040



Internal ID18782571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30656421..30795118hg38UCSC Ensembl
Innerchr15:30948624..31087321hg19UCSC Ensembl
Innerchr15:28735916..28874613hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38138698
hg19138698
hg18138698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2533n100
Supporting Variantsnssv3547650
Samples
Known GenesLOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040040
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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