A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6201739



Internal ID9723550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67747469..67755720hg38UCSC Ensembl
chr13:68321601..68329852hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg388252
hg198252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675960
Supporting Variants
SamplesNA19474
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6201739
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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