A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6328689



Internal ID9405383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15977153..15986011hg38UCSC Ensembl
Outerchr19:15976996..15986164hg38UCSC Ensembl
Innerchr19:16087963..16096821hg19UCSC Ensembl
Outerchr19:16087806..16096974hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg389169
hg199169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678800
Supporting Variants
SamplesNA18610
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6328689
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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