A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660700



Internal ID9580119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7848726..7849399hg38UCSC Ensembl
Outerchr1:7848692..7849434hg38UCSC Ensembl
Innerchr1:7908786..7909459hg19UCSC Ensembl
Outerchr1:7908752..7909494hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5452478
SamplesHG00310
Known GenesUTS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660700
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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