A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668188



Internal ID9934293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77267923..77277155hg38UCSC Ensembl
Outerchr17:77267886..77277205hg38UCSC Ensembl
Innerchr17:75264005..75273237hg19UCSC Ensembl
Outerchr17:75263968..75273287hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg389320
hg199320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv568e199
Supporting Variantsessv5696647, essv6211404, essv5543717, essv6075993, essv6442969, essv5925844, essv5740834, essv6372730, essv5468820
SamplesHG00231, NA20766, NA12341, HG01168, NA19725, HG01101, HG01190, NA20807, NA07056
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668188
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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