A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893521



Internal ID19184341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:187202628..187300439hg38UCSC Ensembl
Outerchr2:187202628..187300439hg38UCSC Ensembl
Innerchr2:188067355..188165166hg19UCSC Ensembl
Outerchr2:188067355..188165166hg19UCSC Ensembl
Innerchr2:187775600..187873411hg18UCSC Ensembl
Outerchr2:187775600..187873411hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3897812
hg1997812
hg1897812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785206
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893521
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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