A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893566



Internal ID19184386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231429669..231436959hg38UCSC Ensembl
Outerchr2:231429669..231440068hg38UCSC Ensembl
Innerchr2:232294380..232301670hg19UCSC Ensembl
Outerchr2:232294380..232304779hg19UCSC Ensembl
Innerchr2:232002624..232009914hg18UCSC Ensembl
Outerchr2:232002624..232013023hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3810400
hg1910400
hg1810400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781757, essv25785514
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893566
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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