A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892369



Internal ID18836503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61975570..64334710hg38UCSC Ensembl
Outerchr13:61975570..64334710hg38UCSC Ensembl
Innerchr13:62549703..64908842hg19UCSC Ensembl
Outerchr13:62549703..64908842hg19UCSC Ensembl
Innerchr13:61447704..63806843hg18UCSC Ensembl
Outerchr13:61447704..63806843hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg382359141
hg192359140
hg182359140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797743
Samples
Known GenesLINC00395, MIR548AN, OR7E156P
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892369
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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