A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6428838



Internal ID9096954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:96254405..96260880hg38UCSC Ensembl
Outerchr1:96254248..96261033hg38UCSC Ensembl
Innerchr1:96719961..96726436hg19UCSC Ensembl
Outerchr1:96719804..96726589hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386786
hg196786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658149
Supporting Variants
SamplesHG01079
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6428838
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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