A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891860



Internal ID18839570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38666518..38701839hg38UCSC Ensembl
Outerchr2:38666518..38724524hg38UCSC Ensembl
Innerchr2:38893660..38928981hg19UCSC Ensembl
Outerchr2:38893660..38951666hg19UCSC Ensembl
Innerchr2:38747164..38782485hg18UCSC Ensembl
Outerchr2:38747164..38805170hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3858007
hg1958007
hg1858007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785938, essv25784443, essv25787688
Samples
Known GenesGALM
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891860
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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