A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664651



Internal ID9930756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13664776..13668894hg38UCSC Ensembl
chr3:13706276..13710394hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384119
hg194119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5796145, essv6537035, essv5572542
SamplesNA18871, NA18853, NA19440
Known GenesLINC00620
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664651
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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