A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657858



Internal ID9923963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71587787..71591012hg38UCSC Ensembl
chr15:71880126..71883351hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383226
hg193226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6218864, essv5454255, essv6057220, essv6532815, essv5445230, essv5545178, essv6230700, essv6068035, essv6567785, essv5977793, essv6456397, essv5637399, essv5848322, essv5670556, essv6030462, essv5855268
SamplesNA19648, NA19703, NA19664, NA19914, NA19777, NA19660, NA19728, NA19678, NA19720, NA20278, NA19908, NA19774, NA19682, NA19773, NA19661, NA20322
Known GenesTHSD4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657858
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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