A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661256



Internal ID9580675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:169999401..170001724hg38UCSC Ensembl
Outerchr4:169999364..170001774hg38UCSC Ensembl
Innerchr4:170920552..170922875hg19UCSC Ensembl
Outerchr4:170920515..170922925hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg382411
hg192411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6533488
SamplesNA19723
Known GenesMFAP3L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661256
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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