A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7516952



Internal ID10795234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110313540..110313880hg38UCSC Ensembl
Outerchr13:110965887..110966227hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3247385
Supporting Variants
SamplesHuRef
Known GenesCOL4A2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7516952
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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