A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660119



Internal ID9579538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:71421005..71421226hg38UCSC Ensembl
Outerchr1:71420968..71421276hg38UCSC Ensembl
Innerchr1:71886688..71886909hg19UCSC Ensembl
Outerchr1:71886651..71886959hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6376823
SamplesNA18956
Known GenesNEGR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660119
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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