A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670375



Internal ID9936480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35104011..35109604hg38UCSC Ensembl
Outerchr4:35103974..35109654hg38UCSC Ensembl
Innerchr4:35105633..35111226hg19UCSC Ensembl
Outerchr4:35105596..35111276hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg385681
hg195681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6431135
SamplesHG00245
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670375
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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