A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6087873



Internal ID9785316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39656846..39656952hg38UCSC Ensembl
Outerchr4:39656475..39657322hg38UCSC Ensembl
Innerchr4:39658466..39658572hg19UCSC Ensembl
Outerchr4:39658095..39658942hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666337
Supporting Variants
SamplesNA19776
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6087873
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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