A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892364



Internal ID19183184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61068524..61095595hg38UCSC Ensembl
Outerchr13:61068524..61096625hg38UCSC Ensembl
Innerchr13:61642658..61669729hg19UCSC Ensembl
Outerchr13:61642658..61670759hg19UCSC Ensembl
Innerchr13:60540659..60567730hg18UCSC Ensembl
Outerchr13:60540659..60568760hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3828102
hg1928102
hg1828102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798312, essv25784221, essv25785781
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892364
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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