A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039606



Internal ID19128825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32196661..32356519hg38UCSC Ensembl
Innerchr15:32488862..32648720hg19UCSC Ensembl
Innerchr15:30276154..30436012hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38159859
hg19159859
hg18159859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2541n100
Supporting Variantsnssv3547791, nssv3547790, nssv3547792
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)nsv1039606
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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