A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6105750



Internal ID9083153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10311332..10312441hg38UCSC Ensembl
Outerchr19:10311295..10312491hg38UCSC Ensembl
Innerchr19:10422008..10423117hg19UCSC Ensembl
Outerchr19:10421971..10423167hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667969
Supporting Variants
SamplesNA19661
Known GenesFDX1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6105750
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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