A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891737



Internal ID18839447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1139366..1173213hg38UCSC Ensembl
Outerchr10:1139366..1173213hg38UCSC Ensembl
Innerchr10:1185306..1219153hg19UCSC Ensembl
Outerchr10:1185306..1219153hg19UCSC Ensembl
Innerchr10:1175306..1209153hg18UCSC Ensembl
Outerchr10:1175306..1209153hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3833848
hg1933848
hg1833848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789161
Samples
Known GenesLINC00200
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891737
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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