A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791166



Internal ID18828622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2700967..3236463hg38UCSC Ensembl
Innerchr8:2558468..3093985hg19UCSC Ensembl
Innerchr8:2545875..3081392hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38535497
hg19535518
hg18535518
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891261
Supporting Variants
Samples
Known GenesCSMD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=292
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791166
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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