A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891581



Internal ID19185977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15138437..15242207hg38UCSC Ensembl
Outerchr2:15138437..15242207hg38UCSC Ensembl
Innerchr2:15278561..15382331hg19UCSC Ensembl
Outerchr2:15278561..15382331hg19UCSC Ensembl
Innerchr2:15196012..15299782hg18UCSC Ensembl
Outerchr2:15196012..15299782hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38103771
hg19103771
hg18103771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785905
Samples
Known GenesNBAS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891581
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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