A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6586893



Internal ID9599626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38954081..38955890hg38UCSC Ensembl
chr13:39528218..39530027hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381810
hg191810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674385
Supporting Variants
SamplesNA19236
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6586893
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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