A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656839



Internal ID9922944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38425193..38429901hg38UCSC Ensembl
Outerchr4:38425036..38430054hg38UCSC Ensembl
Innerchr4:38426814..38431522hg19UCSC Ensembl
Outerchr4:38426657..38431675hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg385019
hg195019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6065896
SamplesNA12249
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656839
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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