A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038450



Internal ID19127669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87358251..87370306hg38UCSC Ensembl
Innerchr15:87901482..87913537hg19UCSC Ensembl
Innerchr15:85702486..85714541hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3812056
hg1912056
hg1812056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555190, nssv3555189
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)nsv1038450
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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