A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892687



Internal ID19183507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46631646..46710871hg38UCSC Ensembl
Outerchr15:46631646..46710871hg38UCSC Ensembl
Innerchr15:46923844..47003069hg19UCSC Ensembl
Outerchr15:46923844..47003069hg19UCSC Ensembl
Innerchr15:44711136..44790361hg18UCSC Ensembl
Outerchr15:44711136..44790361hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3879226
hg1979226
hg1879226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781098
Samples
Known GenesMIR548A3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892687
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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