A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660738



Internal ID9580157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9014165..9545699hg38UCSC Ensembl
chr4:9015891..9547324hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38531535
hg19531434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv922e199
Supporting Variantsessv5884101
SamplesHG01107
Known GenesDEFB131, USP17L10, USP17L11, USP17L12, USP17L13, USP17L15, USP17L17, USP17L18, USP17L19, USP17L20, USP17L21, USP17L22, USP17L24, USP17L25, USP17L26, USP17L27, USP17L28, USP17L29, USP17L30, USP17L5, USP17L6P, USP17L9P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660738
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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