A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656498



Internal ID9922603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174359287..174362850hg38UCSC Ensembl
chr3:174077077..174080640hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg383564
hg193564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5479689, essv5907006, essv6270165, essv5663416, essv5588783, essv6285415
SamplesNA18507, NA19381, NA19449, NA18523, NA18909, NA19147
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656498
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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