A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616737



Internal ID7003623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28381155..28388407hg38UCSC Ensembl
Innerchr8:28381209..28388354hg38UCSC Ensembl
Outerchr8:28381102..28388461hg38UCSC Ensembl
chr8:28238672..28245924hg19UCSC Ensembl
Innerchr8:28238726..28245871hg19UCSC Ensembl
Outerchr8:28238619..28245978hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg387253
hg197253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13153168
SamplesNA19661
Known GenesZNF395
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616737
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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