A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662384



Internal ID9928489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178959733..178964198hg38UCSC Ensembl
Outerchr5:178959667..178964265hg38UCSC Ensembl
Innerchr5:178386734..178391199hg19UCSC Ensembl
Outerchr5:178386668..178391266hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384599
hg194599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1065e199
Supporting Variantsessv5423919, essv6460828
SamplesHG00671, HG01134
Known GenesZNF454
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662384
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer