A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785514



Internal ID19161010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231429669..231440068hg38UCSC Ensembl
Innerchr2:232294380..232304779hg19UCSC Ensembl
Innerchr2:232002624..232013023hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3810400
hg1910400
hg1810400
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893566
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785514
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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