A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797743



Internal ID18833724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61975570..64334710hg38UCSC Ensembl
Innerchr13:62549703..64908842hg19UCSC Ensembl
Innerchr13:61447704..63806843hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg382359141
hg192359140
hg182359140
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892369
Supporting Variants
Samples
Known GenesLINC00395, MIR548AN, OR7E156P
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=317
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797743
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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