A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14674581



Internal ID6849129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26259475..26265941hg38UCSC Ensembl
Innerchr13:26259479..26265938hg38UCSC Ensembl
Outerchr13:26259472..26265945hg38UCSC Ensembl
chr13:26833612..26840078hg19UCSC Ensembl
Innerchr13:26833616..26840075hg19UCSC Ensembl
Outerchr13:26833609..26840082hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg386467
hg196467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631600
Supporting Variants
SamplesNA21086
Known GenesCDK8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14674581
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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