A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668587



Internal ID9588006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8047753..8055359hg38UCSC Ensembl
Outerchr10:8047382..8055729hg38UCSC Ensembl
Innerchr10:8089716..8097322hg19UCSC Ensembl
Outerchr10:8089345..8097692hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg388348
hg198348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv118e199
Supporting Variantsessv5653679, essv5505664, essv5573952, essv5524191, essv5407724, essv6345924, essv6009810, essv5773184, essv5874870, essv5734054, essv6275758, essv6335102, essv5770285, essv6539492, essv6197323, essv5461811, essv5554652, essv6398877, essv6278320, essv5447183, essv6548855, essv6129922, essv6588385, essv5716558, essv5701624, essv6406441, essv6036565, essv6149084, essv6154304
SamplesNA20588, NA20543, NA20514, NA20816, NA20507, NA20771, NA20537, NA20774, NA20518, NA20819, NA20775, NA20811, NA20757, NA20753, NA20818, NA20809, NA20810, NA20536, NA20542, NA20534, NA20522, NA20815, NA20785, NA20790, NA20582, NA20510, NA20826, NA20503, NA20502
Known GenesGATA3, GATA3-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668587
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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