A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044347



Internal ID19133566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41731607..41757162hg38UCSC Ensembl
Innerchr15:42023805..42049360hg19UCSC Ensembl
Innerchr15:39811097..39836652hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3825556
hg1925556
hg1825556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552264
Samples
Known GenesMGA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044347
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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