A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892372



Internal ID19183192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63191227..63228092hg38UCSC Ensembl
Outerchr13:63191227..63228092hg38UCSC Ensembl
Innerchr13:63765360..63802225hg19UCSC Ensembl
Outerchr13:63765360..63802225hg19UCSC Ensembl
Innerchr13:62663361..62700226hg18UCSC Ensembl
Outerchr13:62663361..62700226hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3836866
hg1936866
hg1836866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778691
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892372
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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