A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892697



Internal ID19183517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55430015..55485590hg38UCSC Ensembl
Outerchr15:55430015..55485590hg38UCSC Ensembl
Innerchr15:55722213..55777788hg19UCSC Ensembl
Outerchr15:55722213..55777788hg19UCSC Ensembl
Innerchr15:53509505..53565080hg18UCSC Ensembl
Outerchr15:53509505..53565080hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3855576
hg1955576
hg1855576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786072
Samples
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892697
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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