A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049561



Internal ID18792092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92215204..92554735hg38UCSC Ensembl
Innerchr15:92758434..93097965hg19UCSC Ensembl
Innerchr15:90559438..90898969hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38339532
hg19339532
hg18339532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555226
Samples
Known GenesC15orf32, ST8SIA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049561
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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