A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5907178



Internal ID9564861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17034549..17038452hg38UCSC Ensembl
Outerchr4:17034392..17038605hg38UCSC Ensembl
Innerchr4:17036172..17040075hg19UCSC Ensembl
Outerchr4:17036015..17040228hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg384214
hg194214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657951
Supporting Variants
SamplesNA19108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5907178
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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