A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6330616



Internal ID9192777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55526891..55527080hg38UCSC Ensembl
Outerchr19:55526852..55527137hg38UCSC Ensembl
Innerchr19:56038258..56038447hg19UCSC Ensembl
Outerchr19:56038219..56038504hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665412
Supporting Variants
SamplesHG01489
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6330616
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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