A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6424779



Internal ID9402182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2574157..2575452hg38UCSC Ensembl
chr3:2615841..2617136hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663898
Supporting Variants
SamplesNA19819
Known GenesCNTN4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6424779
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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