A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893520



Internal ID19184340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:186250304..186455765hg38UCSC Ensembl
Outerchr2:186250304..186455765hg38UCSC Ensembl
Innerchr2:187115031..187320492hg19UCSC Ensembl
Outerchr2:187115031..187320492hg19UCSC Ensembl
Innerchr2:186823276..187028737hg18UCSC Ensembl
Outerchr2:186823276..187028737hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38205462
hg19205462
hg18205462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785529
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893520
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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