A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663167



Internal ID9582586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150772343..150776313hg38UCSC Ensembl
Outerchr4:150772306..150776363hg38UCSC Ensembl
Innerchr4:151693495..151697465hg19UCSC Ensembl
Outerchr4:151693458..151697515hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg384058
hg194058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5996871
SamplesNA19474
Known GenesLRBA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663167
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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