A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661911



Internal ID9581330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161561480..161642825hg38UCSC Ensembl
chr1:161531270..161612615hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881346
hg1981346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv75e199
Supporting Variantsessv6036291
SamplesNA18941
Known GenesFCGR2C, FCGR3B, HSPA7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661911
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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