A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038457



Internal ID19127676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45819254..45965990hg38UCSC Ensembl
Innerchr15:46111452..46258188hg19UCSC Ensembl
Innerchr15:43898744..44045480hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38146737
hg19146737
hg18146737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552365
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)nsv1038457
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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