A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890672



Internal ID18838288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95079308..95088343hg38UCSC Ensembl
Outerchr5:95079308..95088343hg38UCSC Ensembl
Innerchr5:94415012..94424047hg19UCSC Ensembl
Outerchr5:94415012..94424047hg19UCSC Ensembl
Innerchr5:94440768..94449803hg18UCSC Ensembl
Outerchr5:94440768..94449803hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg389036
hg199036
hg189036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796495
Samples
Known GenesMCTP1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890672
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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