A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670923



Internal ID9937028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36120379..36121598hg38UCSC Ensembl
Outerchr1:36120342..36121648hg38UCSC Ensembl
Innerchr1:36585980..36587199hg19UCSC Ensembl
Outerchr1:36585943..36587249hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5511753
SamplesNA19138
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670923
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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