A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6435969



Internal ID9413372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9819438..9820577hg38UCSC Ensembl
Outerchr19:9819401..9820627hg38UCSC Ensembl
Innerchr19:9930114..9931253hg19UCSC Ensembl
Outerchr19:9930077..9931303hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662368
Supporting Variants
SamplesHG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6435969
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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