A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893785



Internal ID18837919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149525170..149583818hg38UCSC Ensembl
Outerchr3:149507931..149583818hg38UCSC Ensembl
Innerchr3:149242957..149301605hg19UCSC Ensembl
Outerchr3:149225718..149301605hg19UCSC Ensembl
Innerchr3:150725647..150784295hg18UCSC Ensembl
Outerchr3:150708408..150784295hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3875888
hg1975888
hg1875888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792141, essv25790710
Samples
Known GenesWWTR1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893785
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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