A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784512



Internal ID19169600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:41888256..41901964hg38UCSC Ensembl
Innerchr22:42284260..42297968hg19UCSC Ensembl
Innerchr22:40614206..40627914hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3813709
hg1913709
hg1813709
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893484
Supporting Variants
Samples
Known GenesMIR33A, SREBF2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784512
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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