A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6380795



Internal ID9458752
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
SamplesNA18909
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6380795
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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