A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6459395



Internal ID9692022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96368312..96370218hg38UCSC Ensembl
Outerchr5:96367941..96370588hg38UCSC Ensembl
Innerchr5:95704016..95705922hg19UCSC Ensembl
Outerchr5:95703645..95706292hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382648
hg192648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2669983
Supporting Variants
SamplesNA19443
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6459395
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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