A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5535638



Internal ID9247162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3346412..3349668hg38UCSC Ensembl
Outerchr5:3346237..3349855hg38UCSC Ensembl
Innerchr5:3346526..3349782hg19UCSC Ensembl
Outerchr5:3346351..3349969hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383619
hg193619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672661
Supporting Variants
SamplesNA12044
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5535638
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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