A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661951



Internal ID9928056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:78272975..78274529hg38UCSC Ensembl
Outerchr1:78272938..78274579hg38UCSC Ensembl
Innerchr1:78738659..78740213hg19UCSC Ensembl
Outerchr1:78738622..78740263hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381642
hg191642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6057260
SamplesHG00124
Known GenesMGC27382
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661951
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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