A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660258



Internal ID9926363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16442632..16459101hg38UCSC Ensembl
Outerchr4:16442475..16459254hg38UCSC Ensembl
Innerchr4:16444255..16460724hg19UCSC Ensembl
Outerchr4:16444098..16460877hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3816780
hg1916780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6076256, essv6443226
SamplesNA18618, NA18582
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660258
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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