A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053546



Internal ID19142765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101121007..101150114hg38UCSC Ensembl
Innerchr15:101661212..101690319hg19UCSC Ensembl
Innerchr15:99478735..99507842hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3829108
hg1929108
hg1829108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2671n100
Supporting Variantsnssv3555330
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)nsv1053546
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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