A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5512952



Internal ID9804737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33558662..33564775hg38UCSC Ensembl
chr13:34132799..34138912hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg386114
hg196114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657576
Supporting Variants
SamplesNA19901
Known GenesSTARD13
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5512952
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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