A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5521613



Internal ID8499016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71452353..71461500hg38UCSC Ensembl
Outerchr13:71452316..71461550hg38UCSC Ensembl
Innerchr13:72026485..72035632hg19UCSC Ensembl
Outerchr13:72026448..72035682hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg389235
hg199235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662734
Supporting Variants
SamplesNA19712
Known GenesDACH1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5521613
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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