A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043119



Internal ID19132338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49468025..49552169hg38UCSC Ensembl
Innerchr15:49760222..49844366hg19UCSC Ensembl
Innerchr15:47547514..47631658hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3884145
hg1984145
hg1884145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552381
Samples
Known GenesFAM227B, FGF7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043119
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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