A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5499088



Internal ID8760188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81969188..81978256hg38UCSC Ensembl
Outerchr5:81969151..81978306hg38UCSC Ensembl
Innerchr5:81265007..81274075hg19UCSC Ensembl
Outerchr5:81264970..81274125hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg389156
hg199156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669720
Supporting Variants
SamplesHG00151
Known GenesATG10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5499088
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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