A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892015



Internal ID19186411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44232091..44240933hg38UCSC Ensembl
Outerchr2:44232091..44240933hg38UCSC Ensembl
Innerchr2:44459230..44468072hg19UCSC Ensembl
Outerchr2:44459230..44468072hg19UCSC Ensembl
Innerchr2:44312734..44321576hg18UCSC Ensembl
Outerchr2:44312734..44321576hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg388843
hg198843
hg188843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782708
Samples
Known GenesPPM1B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892015
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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