A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6163460



Internal ID9763234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162396228..162400739hg38UCSC Ensembl
chr5:161823234..161827745hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384512
hg194512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671316
Supporting Variants
SamplesNA19719
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6163460
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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