A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675665



Internal ID9941770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15656672..15657009hg38UCSC Ensembl
chr4:15658295..15658632hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6305538, essv5622241, essv5488956, essv6191495, essv6061186, essv6466599, essv6042602
SamplesNA20532, NA19725, HG01198, NA20818, NA20810, HG01148, NA20815
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675665
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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