A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892705



Internal ID18836839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58414647..58428232hg38UCSC Ensembl
Outerchr15:58414647..58428232hg38UCSC Ensembl
Innerchr15:58706846..58720431hg19UCSC Ensembl
Outerchr15:58706846..58720431hg19UCSC Ensembl
Innerchr15:56494138..56507723hg18UCSC Ensembl
Outerchr15:56494138..56507723hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3813586
hg1913586
hg1813586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801057
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892705
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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