A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043590



Internal ID19132809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183005..71591331hg38UCSC Ensembl
Innerchr15:71475344..71883670hg19UCSC Ensembl
Innerchr15:69262398..69670724hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38408327
hg19408327
hg18408327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553686
Samples
Known GenesTHSD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043590
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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