A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5856628



Internal ID9515844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39484146..39494554hg38UCSC Ensembl
chr13:40058283..40068691hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3810409
hg1910409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677218
Supporting Variants
SamplesNA19002
Known GenesLHFP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5856628
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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