A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6177463



Internal ID9154867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160757165..160759283hg38UCSC Ensembl
Outerchr5:160757008..160759436hg38UCSC Ensembl
Innerchr5:160184172..160186290hg19UCSC Ensembl
Outerchr5:160184015..160186443hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671972
Supporting Variants
SamplesNA19347
Known GenesATP10B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6177463
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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