A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893746



Internal ID18837880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93792469..94164796hg38UCSC Ensembl
Outerchr3:93792469..94164796hg38UCSC Ensembl
Innerchr3:93511313..93883640hg19UCSC Ensembl
Outerchr3:93511313..93883640hg19UCSC Ensembl
Innerchr3:94994003..95366330hg18UCSC Ensembl
Outerchr3:94994003..95366330hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38372328
hg19372328
hg18372328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779409
Samples
Known GenesARL13B, DHFRL1, NSUN3, PROS1, STX19
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893746
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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