A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6242825



Internal ID9441640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112670823..112672043hg38UCSC Ensembl
Innerchr13:113325137..113326357hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674970
Supporting Variants
SamplesNA18853
Known GenesC13orf35
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6242825
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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