A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv914e199



Internal ID20124216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:212699..339559hg38UCSC Ensembl
chr4:206488..333348hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38126861
hg19126861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2665096, esv2662926
SamplesNA19379, HG01048, HG00266, NA19713
Known GenesZNF141, ZNF732, ZNF876P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv914e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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