A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789161



Internal ID18814375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1139366..1173213hg38UCSC Ensembl
Innerchr10:1185306..1219153hg19UCSC Ensembl
Innerchr10:1175306..1209153hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3833848
hg1933848
hg1833848
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891737
Supporting Variants
Samples
Known GenesLINC00200
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789161
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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