A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6464709



Internal ID9529714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100553169..100556509hg38UCSC Ensembl
chr13:101205423..101208763hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg383341
hg193341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672414
Supporting Variants
SamplesNA19059
Known GenesGGACT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6464709
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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