A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892431



Internal ID19183251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95885020..96058284hg38UCSC Ensembl
Outerchr13:95885020..96058284hg38UCSC Ensembl
Innerchr13:96537274..96710538hg19UCSC Ensembl
Outerchr13:96537274..96710538hg19UCSC Ensembl
Innerchr13:95335275..95508539hg18UCSC Ensembl
Outerchr13:95335275..95508539hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38173265
hg19173265
hg18173265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786077
Samples
Known GenesUGGT2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892431
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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