A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6373856



Internal ID8982201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109277004..109279306hg38UCSC Ensembl
Outerchr1:109276967..109279356hg38UCSC Ensembl
Innerchr1:109819626..109821928hg19UCSC Ensembl
Outerchr1:109819589..109821978hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382390
hg192390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669492
Supporting Variants
SamplesHG00577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6373856
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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