A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6301682



Internal ID9653192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100169740..100173850hg38UCSC Ensembl
chr13:100821994..100826104hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384111
hg194111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671626
Supporting Variants
SamplesNA19383
Known GenesPCCA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6301682
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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